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: E9B513
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 | 190 | 194 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.400 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.762 |
CLV_Separin_Metazoa | 227 | 231 | PF03568 | 0.369 |
CLV_Separin_Metazoa | 247 | 251 | PF03568 | 0.193 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.341 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.374 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.290 |
DOC_CYCLIN_RxL_1 | 199 | 211 | PF00134 | 0.315 |
DOC_MAPK_DCC_7 | 244 | 253 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 224 | 231 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.328 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.425 |
DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.413 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.234 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.248 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 250 | 260 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 299 | 307 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.349 |
LIG_Actin_WH2_2 | 130 | 147 | PF00022 | 0.344 |
LIG_AP2alpha_1 | 126 | 130 | PF02296 | 0.344 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.260 |
LIG_BIR_III_2 | 193 | 197 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.390 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.372 |
LIG_CaM_NSCaTE_8 | 14 | 21 | PF13499 | 0.394 |
LIG_CaM_NSCaTE_8 | 382 | 389 | PF13499 | 0.242 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.282 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.425 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.356 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.606 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.366 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.244 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.199 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 62 | 66 | PF02991 | 0.234 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 164 | 172 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 92 | 100 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.280 |
LIG_Pex14_1 | 257 | 261 | PF04695 | 0.397 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.293 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.320 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.292 |
LIG_Rb_pABgroove_1 | 181 | 189 | PF01858 | 0.234 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.443 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.351 |
LIG_SH2_GRB2like | 236 | 239 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 169 | 172 | PF00017 | 0.332 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.242 |
LIG_SH2_STAT3 | 422 | 425 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 77 | 80 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.281 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.348 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.469 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.360 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.725 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.135 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.190 |
LIG_TRAF2_2 | 286 | 291 | PF00917 | 0.369 |
LIG_TYR_ITIM | 118 | 123 | PF00017 | 0.242 |
LIG_TYR_ITIM | 277 | 282 | PF00017 | 0.466 |
LIG_UBA3_1 | 397 | 402 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.359 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.234 |
LIG_WW_3 | 247 | 251 | PF00397 | 0.371 |
MOD_CDK_SPK_2 | 447 | 452 | PF00069 | 0.567 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.400 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.436 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.214 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.573 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.605 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.374 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.297 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.415 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.195 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.391 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.664 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.652 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.285 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.310 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.431 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.356 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.115 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.320 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.582 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.725 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.744 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.285 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.293 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.373 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.355 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.512 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.401 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.411 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.426 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.423 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.260 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.664 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.640 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.183 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.372 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.593 |
MOD_PK_1 | 219 | 225 | PF00069 | 0.328 |
MOD_PK_1 | 293 | 299 | PF00069 | 0.232 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.413 |
MOD_PKA_1 | 299 | 305 | PF00069 | 0.413 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.444 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.307 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.292 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.302 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.466 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.423 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.310 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.624 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.457 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.286 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.460 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.402 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.366 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.307 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.447 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.309 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.565 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.604 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.286 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.301 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.293 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.754 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.696 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.643 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.687 |
MOD_SUMO_rev_2 | 209 | 213 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.301 |
TRG_DiLeu_BaEn_1 | 273 | 278 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_3 | 333 | 339 | PF01217 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.260 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.260 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.305 |
TRG_NES_CRM1_1 | 514 | 530 | PF08389 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.160 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K7 | Leptomonas seymouri | 48% | 90% |
A0A0N0P9A4 | Leptomonas seymouri | 75% | 98% |
A0A0S4KGM0 | Bodo saltans | 48% | 89% |
A0A1X0P6D7 | Trypanosomatidae | 48% | 98% |
A0A1X0P9Q8 | Trypanosomatidae | 64% | 97% |
A0A3R7LDF3 | Trypanosoma rangeli | 45% | 100% |
A0A3S7WV81 | Leishmania donovani | 45% | 85% |
A0A3S7X801 | Leishmania donovani | 91% | 100% |
A0A422P0G8 | Trypanosoma rangeli | 61% | 99% |
A4H9Y5 | Leishmania braziliensis | 47% | 86% |
A4HAT9 | Leishmania braziliensis | 77% | 100% |
A4HY50 | Leishmania infantum | 45% | 85% |
A4IA07 | Leishmania infantum | 91% | 100% |
B3LF48 | Arabidopsis thaliana | 35% | 99% |
C9ZMM9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 86% |
D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ARX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
Q4Q2X3 | Leishmania major | 90% | 100% |
Q4QDJ3 | Leishmania major | 47% | 85% |
Q4V8H8 | Rattus norvegicus | 34% | 99% |
Q5E9R3 | Bos taurus | 34% | 100% |
Q5RBP4 | Pongo abelii | 33% | 100% |
Q641Z6 | Rattus norvegicus | 33% | 100% |
Q8BH64 | Mus musculus | 34% | 99% |
Q8R491 | Rattus norvegicus | 34% | 100% |
Q94CF0 | Arabidopsis thaliana | 35% | 99% |
Q9EQP2 | Mus musculus | 32% | 100% |
Q9H223 | Homo sapiens | 34% | 100% |
Q9H4M9 | Homo sapiens | 33% | 100% |
Q9NZN3 | Homo sapiens | 34% | 100% |
Q9NZN4 | Homo sapiens | 34% | 99% |
Q9QXY6 | Mus musculus | 34% | 100% |
Q9WVK4 | Mus musculus | 33% | 100% |
V5BSA9 | Trypanosoma cruzi | 46% | 100% |
V5DGT0 | Trypanosoma cruzi | 62% | 99% |