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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 10 |
GO:0016020 | membrane | 2 | 10 |
GO:0019866 | organelle inner membrane | 4 | 10 |
GO:0031090 | organelle membrane | 3 | 10 |
GO:0031966 | mitochondrial membrane | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3S7XBS4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.420 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.393 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.337 |
DEG_MDM2_SWIB_1 | 90 | 97 | PF02201 | 0.423 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.236 |
DEG_SPOP_SBC_1 | 15 | 19 | PF00917 | 0.407 |
DEG_SPOP_SBC_1 | 284 | 288 | PF00917 | 0.677 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.592 |
DOC_CYCLIN_RxL_1 | 34 | 47 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 233 | 239 | PF00134 | 0.360 |
DOC_MAPK_DCC_7 | 39 | 48 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 113 | 123 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 170 | 180 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 261 | 267 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 359 | 369 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 116 | 125 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 149 | 156 | PF00069 | 0.320 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 204 | 207 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.360 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.543 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.691 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.368 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 73 | 91 | PF00022 | 0.411 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.384 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.315 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.337 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.412 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.408 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.357 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.543 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.659 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.480 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.383 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.463 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.386 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.396 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.365 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.423 |
LIG_LIR_Gen_1 | 19 | 29 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 92 | 100 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.379 |
LIG_NRBOX | 322 | 328 | PF00104 | 0.420 |
LIG_PCNA_yPIPBox_3 | 424 | 437 | PF02747 | 0.461 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.363 |
LIG_Pex14_2 | 90 | 94 | PF04695 | 0.370 |
LIG_REV1ctd_RIR_1 | 123 | 134 | PF16727 | 0.337 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.414 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.510 |
LIG_SH2_SRC | 179 | 182 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.719 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.415 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.743 |
LIG_SUMO_SIM_anti_2 | 263 | 269 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 11 | 19 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 238 | 245 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 248 | 258 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 44 | 51 | PF11976 | 0.318 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.332 |
LIG_UBA3_1 | 193 | 198 | PF00899 | 0.502 |
LIG_UBA3_1 | 266 | 275 | PF00899 | 0.551 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.346 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.413 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.635 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.639 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.328 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.566 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.629 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.450 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.287 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.393 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.589 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.522 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.571 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.608 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.363 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.423 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.679 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.677 |
MOD_GlcNHglycan | 299 | 303 | PF01048 | 0.576 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.416 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.418 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.557 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.450 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.696 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.404 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.303 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.559 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.675 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.657 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.397 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.587 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.595 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.606 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.383 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.490 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.391 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.405 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.432 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.644 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.532 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.186 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.446 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.317 |
MOD_NEK2_2 | 174 | 179 | PF00069 | 0.337 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.402 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.341 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.332 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.523 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.364 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.453 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.517 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.662 |
MOD_Plk_2-3 | 183 | 189 | PF00069 | 0.319 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.408 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.360 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.390 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.318 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.422 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.373 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.341 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.433 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.595 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.698 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.532 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.473 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.368 |
MOD_SUMO_rev_2 | 50 | 55 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_3 | 189 | 195 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 336 | 341 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.508 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.468 |
TRG_NES_CRM1_1 | 169 | 183 | PF08389 | 0.423 |
TRG_NES_CRM1_1 | 232 | 245 | PF08389 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFP5 | Leptomonas seymouri | 70% | 96% |
A0A0S4IXD9 | Bodo saltans | 32% | 100% |
A0A1X0NQP6 | Trypanosomatidae | 28% | 94% |
A0A1X0P1R2 | Trypanosomatidae | 45% | 81% |
A0A3Q8IUI9 | Leishmania donovani | 29% | 100% |
A0A3R7RKG3 | Trypanosoma rangeli | 44% | 100% |
A0A422MTV6 | Trypanosoma rangeli | 30% | 94% |
A4HAQ0 | Leishmania braziliensis | 27% | 100% |
A4HQ55 | Leishmania braziliensis | 88% | 100% |
A4IDV4 | Leishmania infantum | 100% | 100% |
C9ZVE3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 92% |
D0A462 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 83% |
E9ATX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
F4IQG2 | Arabidopsis thaliana | 28% | 90% |
P32839 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 97% |
Q4Q0M1 | Leishmania major | 94% | 99% |
Q54DY9 | Dictyostelium discoideum | 30% | 97% |
Q54HY8 | Dictyostelium discoideum | 31% | 100% |
Q5E9H5 | Bos taurus | 28% | 100% |
Q7ZTL7 | Xenopus laevis | 28% | 100% |
Q7ZV60 | Danio rerio | 27% | 100% |
Q8GW96 | Arabidopsis thaliana | 29% | 89% |
Q9CZP5 | Mus musculus | 27% | 100% |
Q9FLD5 | Arabidopsis thaliana | 28% | 86% |
Q9LH83 | Arabidopsis thaliana | 26% | 90% |
Q9LJJ7 | Arabidopsis thaliana | 26% | 89% |
Q9LP11 | Arabidopsis thaliana | 28% | 93% |
Q9P6Q3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 99% |
Q9Y276 | Homo sapiens | 27% | 100% |
V5BA71 | Trypanosoma cruzi | 30% | 95% |
V5BUW7 | Trypanosoma cruzi | 47% | 80% |
V5DQN5 | Trypanosoma cruzi | 23% | 85% |