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: A4HEQ4
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 | 0.247 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.208 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.213 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.257 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.225 |
CLV_PCSK_PC7_1 | 153 | 159 | PF00082 | 0.255 |
CLV_PCSK_PC7_1 | 241 | 247 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.225 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.306 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 126 | 132 | PF00134 | 0.510 |
DOC_MAPK_FxFP_2 | 47 | 50 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 21 | 27 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 291 | 299 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 32 | 39 | PF00069 | 0.396 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.414 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.425 |
LIG_Actin_WH2_2 | 306 | 323 | PF00022 | 0.478 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.491 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.453 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.415 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.452 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.392 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.433 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.436 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.360 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.414 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.425 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.548 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.467 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.545 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.477 |
LIG_GBD_Chelix_1 | 155 | 163 | PF00786 | 0.316 |
LIG_HP1_1 | 33 | 37 | PF01393 | 0.439 |
LIG_KLC1_Yacidic_2 | 140 | 144 | PF13176 | 0.516 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.419 |
LIG_LYPXL_SIV_4 | 223 | 231 | PF13949 | 0.356 |
LIG_MYND_1 | 264 | 268 | PF01753 | 0.481 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.406 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.330 |
LIG_SH2_GRB2like | 224 | 227 | PF00017 | 0.425 |
LIG_SH2_PTP2 | 308 | 311 | PF00017 | 0.382 |
LIG_SH2_SRC | 142 | 145 | PF00017 | 0.465 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.414 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.427 |
LIG_SUMO_SIM_par_1 | 183 | 191 | PF11976 | 0.416 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.516 |
LIG_TYR_ITIM | 306 | 311 | PF00017 | 0.397 |
MOD_CDK_SPxxK_3 | 264 | 271 | PF00069 | 0.394 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.266 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.313 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.279 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.251 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.325 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.378 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.325 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.266 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.306 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.294 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.358 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.292 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.303 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.295 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.405 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.303 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.371 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.266 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.276 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.228 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.303 |
MOD_NEK2_2 | 122 | 127 | PF00069 | 0.361 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.384 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.441 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.361 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.389 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.349 |
MOD_Plk_2-3 | 60 | 66 | PF00069 | 0.170 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.272 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.254 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.270 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.341 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.191 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.355 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.236 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.283 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.244 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.183 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1L3 | Leptomonas seymouri | 81% | 98% |
A0A0S4JJ66 | Bodo saltans | 38% | 100% |
A0A1X0NSR0 | Trypanosomatidae | 60% | 100% |
A0A3S5H7F7 | Leishmania donovani | 90% | 100% |
A0A3S7WSM7 | Leishmania donovani | 25% | 100% |
A0A3S7WZ40 | Leishmania donovani | 28% | 100% |
A0A422NVI7 | Trypanosoma rangeli | 63% | 100% |
A0A422P226 | Trypanosoma rangeli | 27% | 100% |
A4HVQ6 | Leishmania infantum | 25% | 100% |
A4I1I3 | Leishmania infantum | 28% | 100% |
A4I1Y3 | Leishmania infantum | 90% | 100% |
A6H7F2 | Bos taurus | 32% | 100% |
C9ZJY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZS35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
D4A7C0 | Rattus norvegicus | 33% | 100% |
E9AXL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AY30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O14443 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 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% | 87% |
Q06543 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q08726 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 96% |
Q0P5E2 | Bos taurus | 27% | 100% |
Q4IQT8 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 25% | 100% |
Q4PF70 | Ustilago maydis (strain 521 / FGSC 9021) | 25% | 100% |
Q4Q9E3 | Leishmania major | 88% | 98% |
Q4Q9V4 | Leishmania major | 28% | 100% |
Q4R579 | Macaca fascicularis | 32% | 100% |
Q4WT40 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 100% |
Q54NK8 | Dictyostelium discoideum | 28% | 100% |
Q54TE7 | Dictyostelium discoideum | 28% | 100% |
Q56XY2 | Arabidopsis thaliana | 33% | 100% |
Q58DD9 | Sus scrofa | 33% | 100% |
Q5BJ53 | Xenopus tropicalis | 31% | 100% |
Q66KF6 | Xenopus laevis | 32% | 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) | 31% | 100% |
Q6PUR6 | Danio rerio | 34% | 100% |
Q750Q9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 100% |
Q8VEJ1 | Mus musculus | 33% | 100% |
Q9H9Y4 | Homo sapiens | 32% | 100% |
Q9UTL7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
V5DR44 | Trypanosoma cruzi | 60% | 100% |