← Leaderboards
L. Mario Amzel
Johns Hopkins University
$6,369,090
Attributed
$10,356,529
Total exposure
11
Grants
4
Lead (contact PI)
Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants.
Funding over time
peak $1.7M · FY2005–19$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
Funding mix
By agency
NIH$10,356,529 · 11
By mechanism
R01$10,026,092 · 6
P01$310,393 · 1
P41$15,044 · 3
R13$5,000 · 1
Top collaborators
- Nancy Carrasco5 shared
- Richard Aldrich4 shared
- Gordon Frank Tomaselli4 shared
Most similar at Johns Hopkins University
Same institution · by research overlap
- Mi-Hyeon Jang$6,529,728
- Andrew A Pieper$7,901,653
- Kaikobad J. Irani$9,796,643
- Fengyi Wan$4,781,422
- Barry D. Nelkin$6,545,708
Others in their field
Top investigators on “X Ray Crystallography”
- Ian A Wilson · Scripps Research Institute, The$74,286,713
- Andrzej Joachimiak Joachimiak · University Of Chicago$63,589,020
- Ernest Fontes · Cornell University$53,099,382
- John L Markley · University Of Wisconsin Madison$51,043,290
- Wah Chiu · Baylor College Of Medicine$49,962,825
- Joel D Brock · Cornell University$47,686,738
Research focus
X Ray CrystallographyEnzyme StructureEnzyme MechanismBaseAffinityStructurePublic Health RelevanceRegulationMolecularSite Directed MutagenesisMediatingPhysiologicalBindingElectrophysiology (Science)ProteinsChemical KineticsMutationFamilyGrowthCellsMutantDesignCardiacDrug Design /Synthesis /Production
Grant awards (29)
Calmodulin Regulation Na Channels: From Function and Structure to Disease$1,057,247
R01 · FY2019 · HL · contact PI
Mechanism of I-transport by the Na+/I-symporter (NIS)$480,026
R01 · FY2019 · GM
Mechanism of I- transport by the Na+/I- symporter (NIS)$96,712
R01 · FY2019 · GM
Calmodulin Regulation Na Channels: From Function and Structure to Disease$1,057,247
R01 · FY2018 · HL · contact PI
Mechanism of I-transport by the Na+/I-symporter (NIS)$568,786
R01 · FY2018 · GM
Calmodulin Regulation Na Channels: From Function and Structure to Disease$1,057,247
R01 · FY2017 · HL
Mechanism of I-transport by the Na+/I-symporter (NIS)$574,261
R01 · FY2017 · GM
Calmodulin Regulation Na Channels: From Function and Structure to Disease$1,072,747
R01 · FY2016 · HL
Mechanism of I-transport by the Na+/I-symporter (NIS)$595,776
R01 · FY2016 · GM
Redox signaling in axon guidance: Structure and activity of MICAL$409,808
R01 · FY2010 · NS · contact PI
The 3rd Latin American Protein Society Meeting (LAPSM)$5,000
R13 · FY2010 · GM · contact PI
Redox signaling in axon guidance: Structure and activity of MICAL$383,702
R01 · FY2009 · NS · contact PI
Structure, Function and Mechanism of Nudix Hydrolases$280,998
R01 · FY2006 · GM · contact PI
Structure, Function and Mechanism of Nudix Hydrolases$287,760
R01 · FY2005 · GM
STRUCTURE AND MECHANISMS OF NAD (P): QUINONE REDUCTASE$245,250
R01 · FY2005 · GM
NADH HUMAN QUINONE REDUCTASE$11,152
P41 · FY2005 · RR
LOCAL CONFORMATIONAL SIMILARITY OF NATIVE AND DENATURED STATE ENSEMBLES$1,945
P41 · FY2005 · RR
Structure, Function and Mechanism of Nudix Hydrolases$287,760
R01 · FY2004 · GM
STRUCTURE AND MECHANISMS OF NAD (P): QUINONE REDUCTASE$245,250
R01 · FY2004 · GM
PEPTIDYL-ALPHA-HYDROXYLATING MONOOXYGENASE (PHM)$1,947
P41 · FY2004 · RR
Structure, Function and Mechanism of Nudix Hydrolases$283,569
R01 · FY2003 · GM
STRUCTURE AND MECHANISMS OF NAD (P): QUINONE REDUCTASE$245,250
R01 · FY2003 · GM
STRUCTURE AND MECHANISMS OF NAD (P): QUINONE REDUCTASE$40,000
R01 · FY2003 · GM
STRUCTURE AND MECHANISMS OF NAD (P): QUINONE REDUCTASE$245,250
R01 · FY2002 · GM
STRUCTURE AND MECHANISM OF LIPOXYGENASE$181,016
R01 · FY2001 · GM
STRUCTURE OF ANTIBODY COMPLEXES WITH BIOACTIVE PEPTIDES$183,097
P01 · FY2000 · GM
STRUCTURE AND MECHANISM OF LIPOXYGENASE$175,838
R01 · FY2000 · GM
STRUCTURE AND MECHANISMS OF NAD(P)--QUINONE REDUCTASE$154,592
R01 · FY2000 · GM
STRUCTURE OF ANTIBODY COMPLEXES WITH BIOACTIVE PEPTIDES$127,296
P01 · FY2000 · GM