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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0019866 | organelle inner membrane | 4 | 9 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0031966 | mitochondrial membrane | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4Q0M1
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0016887 | ATP hydrolysis activity | 7 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.359 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.309 |
CLV_PCSK_FUR_1 | 164 | 168 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.123 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 165 | 173 | PF00400 | 0.328 |
DEG_MDM2_SWIB_1 | 84 | 91 | PF02201 | 0.421 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.240 |
DOC_CKS1_1 | 268 | 273 | PF01111 | 0.376 |
DOC_CYCLIN_RxL_1 | 34 | 47 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 227 | 233 | PF00134 | 0.352 |
DOC_MAPK_DCC_7 | 39 | 48 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 107 | 117 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 255 | 261 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 353 | 363 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 143 | 150 | PF00069 | 0.311 |
DOC_PP1_RVXF_1 | 357 | 364 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.383 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.352 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.123 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.372 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 67 | 85 | PF00022 | 0.415 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.323 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.328 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.410 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.396 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.352 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.454 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.376 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.382 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.309 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.391 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.418 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 193 | 201 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 21 | 29 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.337 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.309 |
LIG_PCNA_yPIPBox_3 | 418 | 431 | PF02747 | 0.473 |
LIG_Pex14_1 | 202 | 206 | PF04695 | 0.351 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.363 |
LIG_REV1ctd_RIR_1 | 117 | 128 | PF16727 | 0.328 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.422 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.530 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.398 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.421 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.682 |
LIG_SUMO_SIM_anti_2 | 257 | 263 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 11 | 18 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 232 | 239 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 242 | 252 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.211 |
LIG_SUMO_SIM_par_1 | 333 | 339 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 44 | 51 | PF11976 | 0.309 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.323 |
LIG_UBA3_1 | 187 | 192 | PF00899 | 0.495 |
LIG_UBA3_1 | 260 | 269 | PF00899 | 0.454 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.339 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.309 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.360 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.268 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.182 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.588 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.661 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.454 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.297 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.400 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.623 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.653 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.357 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.392 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.205 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.419 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.415 |
MOD_GlcNHglycan | 293 | 297 | PF01048 | 0.240 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.219 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.265 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.657 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.555 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.410 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.309 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.467 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.410 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.356 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.319 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.642 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.489 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.438 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.370 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.421 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.393 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.342 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.421 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.123 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.430 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.287 |
MOD_NEK2_2 | 168 | 173 | PF00069 | 0.352 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.352 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.323 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.454 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.680 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.323 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.549 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.698 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.421 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.338 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.321 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.420 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.366 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.453 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.384 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.405 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.582 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.470 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.372 |
MOD_SUMO_rev_2 | 50 | 55 | PF00179 | 0.407 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.309 |
TRG_DiLeu_BaEn_3 | 183 | 189 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.352 |
TRG_DiLeu_BaLyEn_6 | 416 | 421 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.600 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 254 | 256 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.328 |
TRG_NES_CRM1_1 | 163 | 177 | PF08389 | 0.421 |
TRG_NES_CRM1_1 | 226 | 239 | PF08389 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFP5 | Leptomonas seymouri | 69% | 95% |
A0A0S4IXD9 | Bodo saltans | 30% | 100% |
A0A0S4IXV8 | Bodo saltans | 29% | 95% |
A0A1X0NQP6 | Trypanosomatidae | 29% | 92% |
A0A1X0P1R2 | Trypanosomatidae | 45% | 79% |
A0A3Q8IUI9 | Leishmania donovani | 29% | 100% |
A0A3R7RKG3 | Trypanosoma rangeli | 47% | 100% |
A0A3S7XBS4 | Leishmania donovani | 94% | 99% |
A0A422MTV6 | Trypanosoma rangeli | 30% | 93% |
A4HAQ0 | Leishmania braziliensis | 29% | 100% |
A4HQ55 | Leishmania braziliensis | 86% | 80% |
A4IDV4 | Leishmania infantum | 94% | 75% |
C9ZVE3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 91% |
D0A462 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 82% |
E9ATX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 73% |
E9B4V7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P32839 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 96% |
Q4Q369 | Leishmania major | 29% | 100% |
Q54DY9 | Dictyostelium discoideum | 31% | 95% |
Q54HY8 | Dictyostelium discoideum | 31% | 100% |
Q5E9H5 | Bos taurus | 29% | 100% |
Q7ZTL7 | Xenopus laevis | 29% | 100% |
Q7ZV60 | Danio rerio | 28% | 100% |
Q8GW96 | Arabidopsis thaliana | 30% | 88% |
Q9CZP5 | Mus musculus | 28% | 100% |
Q9FN77 | Arabidopsis thaliana | 27% | 82% |
Q9LH83 | Arabidopsis thaliana | 26% | 89% |
Q9LP11 | Arabidopsis thaliana | 27% | 92% |
Q9P6Q3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 97% |
Q9Y276 | Homo sapiens | 28% | 100% |
V5BA71 | Trypanosoma cruzi | 30% | 93% |
V5BUW7 | Trypanosoma cruzi | 48% | 79% |
V5DQN5 | Trypanosoma cruzi | 24% | 84% |