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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9AY30
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.264 |
CLV_PCSK_PC7_1 | 145 | 151 | PF00082 | 0.292 |
CLV_PCSK_PC7_1 | 233 | 239 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.264 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.360 |
DOC_CKS1_1 | 257 | 262 | PF01111 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.534 |
DOC_MAPK_FxFP_2 | 47 | 50 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 116 | 125 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 21 | 27 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 283 | 291 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 32 | 39 | PF00069 | 0.432 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.538 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.452 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.464 |
LIG_Actin_WH2_2 | 298 | 315 | PF00022 | 0.510 |
LIG_eIF4E_1 | 282 | 288 | PF01652 | 0.528 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.531 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.476 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.404 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.445 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.422 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.616 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.488 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.454 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.395 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.452 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.464 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.464 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.707 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.555 |
LIG_GBD_Chelix_1 | 147 | 155 | PF00786 | 0.338 |
LIG_HP1_1 | 33 | 37 | PF01393 | 0.477 |
LIG_KLC1_Yacidic_2 | 132 | 136 | PF13176 | 0.538 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.435 |
LIG_MYND_1 | 256 | 260 | PF01753 | 0.570 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.463 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.372 |
LIG_SH2_GRB2like | 216 | 219 | PF00017 | 0.540 |
LIG_SH2_PTP2 | 300 | 303 | PF00017 | 0.507 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.501 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.452 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.453 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.263 |
LIG_SUMO_SIM_par_1 | 175 | 183 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 270 | 275 | PF11976 | 0.581 |
LIG_TRAF2_1 | 259 | 262 | PF00917 | 0.613 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.519 |
MOD_CDK_SPxxK_3 | 256 | 263 | PF00069 | 0.609 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.317 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.329 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.305 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.305 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.572 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.320 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.320 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.636 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.245 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.333 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.339 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.603 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.320 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.567 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.320 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.296 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.274 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.498 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.393 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.433 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.493 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.401 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.540 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.305 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.121 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.511 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.320 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.387 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.232 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 92 | 95 | PF00179 | 0.277 |
TRG_DiLeu_BaEn_1 | 293 | 298 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.264 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1L3 | Leptomonas seymouri | 80% | 95% |
A0A0S4JJ66 | Bodo saltans | 39% | 100% |
A0A1X0NNN3 | Trypanosomatidae | 30% | 100% |
A0A1X0NSR0 | Trypanosomatidae | 63% | 100% |
A0A3S5H7F7 | Leishmania donovani | 97% | 100% |
A0A3S7WZ40 | Leishmania donovani | 29% | 100% |
A0A422NVI7 | Trypanosoma rangeli | 65% | 100% |
A0A422P226 | Trypanosoma rangeli | 26% | 100% |
A4H7B1 | Leishmania braziliensis | 25% | 100% |
A4HEQ4 | Leishmania braziliensis | 90% | 100% |
A4I1I3 | Leishmania infantum | 29% | 100% |
A4I1Y3 | Leishmania infantum | 97% | 100% |
A6H7F2 | Bos taurus | 33% | 100% |
C9ZJY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZS35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
D4A7C0 | Rattus norvegicus | 34% | 100% |
E9AXL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
O14443 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
P0CN94 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 24% | 100% |
P0CN95 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 24% | 100% |
P47122 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 85% |
Q06543 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q08726 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 94% |
Q4IQT8 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 27% | 100% |
Q4PF70 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |
Q4Q9E3 | Leishmania major | 95% | 100% |
Q4Q9V4 | Leishmania major | 29% | 100% |
Q4R579 | Macaca fascicularis | 34% | 100% |
Q4WT40 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 100% |
Q54NK8 | Dictyostelium discoideum | 30% | 100% |
Q54TE7 | Dictyostelium discoideum | 30% | 100% |
Q56XY2 | Arabidopsis thaliana | 34% | 100% |
Q58DD9 | Sus scrofa | 34% | 100% |
Q5BJ53 | Xenopus tropicalis | 31% | 100% |
Q66KF6 | Xenopus laevis | 33% | 100% |
Q6CQA6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
Q6FSS0 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 32% | 100% |
Q6PUR6 | Danio rerio | 34% | 100% |
Q750Q9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q8VEJ1 | Mus musculus | 34% | 100% |
Q9H9Y4 | Homo sapiens | 34% | 100% |
Q9UTL7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
V5B835 | Trypanosoma cruzi | 31% | 100% |
V5DR44 | Trypanosoma cruzi | 63% | 100% |