Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H7G7
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003924 | GTPase activity | 7 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005525 | GTP binding | 5 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0019001 | guanyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.516 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.393 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.356 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.525 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.384 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.364 |
LIG_14-3-3_CanoR_1 | 116 | 125 | PF00244 | 0.496 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.276 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.343 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.303 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.441 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.450 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.340 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 91 | 100 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.458 |
LIG_SH2_STAT3 | 117 | 120 | PF00017 | 0.425 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.427 |
LIG_SUMO_SIM_anti_2 | 161 | 167 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 45 | 50 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 164 | 170 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 47 | 53 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 60 | 66 | PF11976 | 0.409 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.425 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.477 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.255 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.353 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.414 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.356 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.341 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.397 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.339 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.497 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.427 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.333 |
MOD_PIKK_1 | 116 | 122 | PF00454 | 0.446 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.479 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.474 |
MOD_PK_1 | 137 | 143 | PF00069 | 0.492 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.487 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.308 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.388 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.252 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.352 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.390 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.371 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.546 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 53 | 61 | PF00179 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBE8 | Leptomonas seymouri | 63% | 78% |
A0A1X0NNU1 | Trypanosomatidae | 36% | 100% |
A0A3R7LA27 | Trypanosoma rangeli | 44% | 100% |
A0A3S7WSS1 | Leishmania donovani | 87% | 100% |
A4HVU8 | Leishmania infantum | 87% | 100% |
C9ZT78 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9APK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QFX9 | Leishmania major | 84% | 100% |
V5DE15 | Trypanosoma cruzi | 43% | 100% |