Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 9 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 22 |
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HAT9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0016197 | endosomal transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005525 | GTP binding | 5 | 22 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0019001 | guanyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.300 |
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.314 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 68 | 70 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 390 | 392 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 68 | 70 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.337 |
CLV_Separin_Metazoa | 238 | 242 | PF03568 | 0.367 |
CLV_Separin_Metazoa | 258 | 262 | PF03568 | 0.193 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.340 |
DEG_APCC_DBOX_1 | 370 | 378 | PF00400 | 0.373 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.432 |
DEG_ODPH_VHL_1 | 149 | 160 | PF01847 | 0.314 |
DOC_AGCK_PIF_2 | 175 | 180 | PF00069 | 0.153 |
DOC_CKS1_1 | 161 | 166 | PF01111 | 0.289 |
DOC_CKS1_1 | 480 | 485 | PF01111 | 0.587 |
DOC_MAPK_DCC_7 | 255 | 264 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 176 | 183 | PF00069 | 0.322 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 326 | 333 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 387 | 396 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 421 | 429 | PF00069 | 0.541 |
DOC_MAPK_gen_1 | 66 | 74 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 310 | 319 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 326 | 333 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 154 | 161 | PF00149 | 0.412 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.233 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.235 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 255 | 259 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 303 | 309 | PF00244 | 0.286 |
LIG_14-3-3_CanoR_1 | 356 | 365 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.358 |
LIG_Actin_WH2_2 | 141 | 158 | PF00022 | 0.343 |
LIG_AP2alpha_1 | 137 | 141 | PF02296 | 0.343 |
LIG_APCC_ABBA_1 | 108 | 113 | PF00400 | 0.259 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 378 | 382 | PF00533 | 0.371 |
LIG_CaM_NSCaTE_8 | 25 | 32 | PF13499 | 0.403 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.281 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.356 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.424 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.552 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.284 |
LIG_LIR_Apic_2 | 265 | 271 | PF02991 | 0.377 |
LIG_LIR_Apic_2 | 73 | 77 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 103 | 111 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 179 | 188 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 276 | 284 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 287 | 298 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.282 |
LIG_LRP6_Inhibitor_1 | 429 | 435 | PF00058 | 0.349 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.394 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.292 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.319 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.291 |
LIG_Rb_pABgroove_1 | 192 | 200 | PF01858 | 0.233 |
LIG_SH2_CRK | 243 | 247 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 180 | 183 | PF00017 | 0.330 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 51 | 55 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.280 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.347 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.290 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.468 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.733 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.359 |
LIG_TRAF2_2 | 297 | 302 | PF00917 | 0.365 |
LIG_TYR_ITIM | 288 | 293 | PF00017 | 0.467 |
LIG_UBA3_1 | 408 | 413 | PF00899 | 0.469 |
LIG_WRC_WIRS_1 | 264 | 269 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 71 | 76 | PF05994 | 0.233 |
LIG_WW_3 | 258 | 262 | PF00397 | 0.370 |
LIG_WW_3 | 456 | 460 | PF00397 | 0.444 |
MOD_CDC14_SPxK_1 | 456 | 459 | PF00782 | 0.442 |
MOD_CDK_SPxK_1 | 453 | 459 | PF00069 | 0.443 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.207 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.606 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.504 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.593 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.540 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.413 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.400 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.254 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.314 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.730 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.758 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.284 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.292 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.309 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.530 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.324 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.684 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.737 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.655 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.284 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.534 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.354 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.284 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.513 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.416 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.397 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.425 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.410 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.670 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.259 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.153 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.371 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.612 |
MOD_PK_1 | 230 | 236 | PF00069 | 0.325 |
MOD_PK_1 | 304 | 310 | PF00069 | 0.231 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.412 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.441 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.306 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.475 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.300 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.476 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.635 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.494 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.285 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.405 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.363 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.306 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.446 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.598 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.623 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.308 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.285 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.300 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.292 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.743 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.691 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.637 |
TRG_DiLeu_BaEn_1 | 189 | 194 | PF01217 | 0.300 |
TRG_DiLeu_BaEn_1 | 284 | 289 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_3 | 344 | 350 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.259 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.304 |
TRG_NES_CRM1_1 | 286 | 302 | PF08389 | 0.400 |
TRG_NES_CRM1_1 | 525 | 541 | PF08389 | 0.669 |
TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.288 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.159 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K7 | Leptomonas seymouri | 48% | 91% |
A0A0N0P9A4 | Leptomonas seymouri | 75% | 99% |
A0A0S4KGM0 | Bodo saltans | 48% | 89% |
A0A1X0P6D7 | Trypanosomatidae | 51% | 99% |
A0A1X0P9Q8 | Trypanosomatidae | 64% | 98% |
A0A3R7LDF3 | Trypanosoma rangeli | 46% | 100% |
A0A3S7WV81 | Leishmania donovani | 46% | 86% |
A0A3S7X801 | Leishmania donovani | 78% | 100% |
A0A422P0G8 | Trypanosoma rangeli | 62% | 100% |
A4H9Y5 | Leishmania braziliensis | 44% | 100% |
A4HY50 | Leishmania infantum | 46% | 86% |
A4IA07 | Leishmania infantum | 78% | 100% |
B3LF48 | Arabidopsis thaliana | 37% | 100% |
C9ZMM9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 87% |
D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ARX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 87% |
E9B513 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q2X3 | Leishmania major | 77% | 100% |
Q4QDJ3 | Leishmania major | 42% | 100% |
Q4V8H8 | Rattus norvegicus | 34% | 100% |
Q5E9R3 | Bos taurus | 33% | 100% |
Q5RBP4 | Pongo abelii | 34% | 100% |
Q641Z6 | Rattus norvegicus | 34% | 100% |
Q8BH64 | Mus musculus | 34% | 100% |
Q8R491 | Rattus norvegicus | 33% | 100% |
Q94CF0 | Arabidopsis thaliana | 37% | 100% |
Q9EQP2 | Mus musculus | 33% | 100% |
Q9H223 | Homo sapiens | 33% | 100% |
Q9H4M9 | Homo sapiens | 34% | 100% |
Q9NZN3 | Homo sapiens | 33% | 100% |
Q9NZN4 | Homo sapiens | 34% | 100% |
Q9QXY6 | Mus musculus | 33% | 100% |
Q9WVK4 | Mus musculus | 34% | 100% |
V5BSA9 | Trypanosoma cruzi | 49% | 100% |
V5DGT0 | Trypanosoma cruzi | 62% | 99% |