Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | 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: A4IA07
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 | 0.443 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.807 |
CLV_Separin_Metazoa | 227 | 231 | PF03568 | 0.404 |
CLV_Separin_Metazoa | 247 | 251 | PF03568 | 0.232 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.385 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.422 |
DEG_SPOP_SBC_1 | 468 | 472 | PF00917 | 0.589 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.364 |
DOC_CYCLIN_RxL_1 | 199 | 211 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.352 |
DOC_MAPK_gen_1 | 410 | 418 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 387 | 394 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.511 |
DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.496 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.283 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.296 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.370 |
DOC_USP7_UBL2_3 | 417 | 421 | PF12436 | 0.624 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.736 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 250 | 260 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 299 | 307 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 434 | 439 | PF00244 | 0.737 |
LIG_Actin_WH2_2 | 130 | 147 | PF00022 | 0.428 |
LIG_AP2alpha_1 | 126 | 130 | PF02296 | 0.459 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.309 |
LIG_APCC_ABBAyCdc20_2 | 204 | 210 | PF00400 | 0.333 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BIR_III_2 | 193 | 197 | PF00653 | 0.528 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.424 |
LIG_CaM_NSCaTE_8 | 14 | 21 | PF13499 | 0.429 |
LIG_CaM_NSCaTE_8 | 382 | 389 | PF13499 | 0.290 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.372 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.474 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.406 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.417 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.608 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.409 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.292 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.303 |
LIG_LIR_Apic_2 | 254 | 260 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 62 | 66 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 164 | 172 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 276 | 287 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 39 | 50 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 92 | 100 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.164 |
LIG_NRBOX | 74 | 80 | PF00104 | 0.222 |
LIG_Pex14_1 | 257 | 261 | PF04695 | 0.441 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.408 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.366 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.244 |
LIG_Rb_pABgroove_1 | 181 | 189 | PF01858 | 0.299 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.551 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.386 |
LIG_SH2_GRB2like | 236 | 239 | PF00017 | 0.503 |
LIG_SH2_PTP2 | 169 | 172 | PF00017 | 0.408 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.290 |
LIG_SH2_STAT3 | 422 | 425 | PF00017 | 0.586 |
LIG_SH2_STAT3 | 77 | 80 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.331 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.419 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.516 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.359 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.409 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.808 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.271 |
LIG_TRAF2_2 | 286 | 291 | PF00917 | 0.410 |
LIG_TYR_ITIM | 118 | 123 | PF00017 | 0.348 |
LIG_TYR_ITIM | 277 | 282 | PF00017 | 0.509 |
LIG_UBA3_1 | 397 | 402 | PF00899 | 0.516 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.283 |
LIG_WW_3 | 247 | 251 | PF00397 | 0.409 |
MOD_CDK_SPK_2 | 447 | 452 | PF00069 | 0.608 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.448 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.290 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.639 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.669 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.370 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.467 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.619 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.696 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.692 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.342 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.392 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.542 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.379 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.346 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.757 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.781 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.339 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.337 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.408 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.486 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.397 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.447 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.284 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.448 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.413 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.309 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.533 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.440 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.612 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.654 |
MOD_PK_1 | 219 | 225 | PF00069 | 0.374 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.461 |
MOD_PKA_1 | 299 | 305 | PF00069 | 0.461 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.356 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.341 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.680 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.359 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.499 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.290 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.359 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.668 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.641 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.371 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.493 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.430 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.411 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.355 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.496 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.355 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.591 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.603 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.324 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.350 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.365 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.776 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.683 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.735 |
MOD_SUMO_rev_2 | 209 | 213 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_1 | 273 | 278 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_3 | 333 | 339 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 314 | 317 | PF00400 | 0.353 |
TRG_NES_CRM1_1 | 514 | 530 | PF08389 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K7 | Leptomonas seymouri | 47% | 91% |
A0A0N0P9A4 | Leptomonas seymouri | 74% | 98% |
A0A0S4KGM0 | Bodo saltans | 48% | 89% |
A0A1X0P6D7 | Trypanosomatidae | 50% | 99% |
A0A1X0P9Q8 | Trypanosomatidae | 62% | 97% |
A0A3R7LDF3 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WV81 | Leishmania donovani | 46% | 86% |
A0A3S7X801 | Leishmania donovani | 100% | 100% |
A0A422P0G8 | Trypanosoma rangeli | 60% | 99% |
A4H9Y5 | Leishmania braziliensis | 46% | 86% |
A4HAT9 | Leishmania braziliensis | 78% | 100% |
A4HY50 | Leishmania infantum | 46% | 86% |
B3LF48 | Arabidopsis thaliana | 35% | 99% |
C9ZMM9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 87% |
D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ARX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 86% |
E9B513 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q2X3 | Leishmania major | 94% | 100% |
Q4QDJ3 | Leishmania major | 45% | 85% |
Q4V8H8 | Rattus norvegicus | 34% | 100% |
Q5E9R3 | Bos taurus | 34% | 100% |
Q5RBP4 | Pongo abelii | 34% | 100% |
Q641Z6 | Rattus norvegicus | 34% | 100% |
Q94CF0 | Arabidopsis thaliana | 36% | 99% |
Q9H223 | Homo sapiens | 34% | 100% |
Q9H4M9 | Homo sapiens | 34% | 100% |
Q9NZN4 | Homo sapiens | 33% | 100% |
Q9WVK4 | Mus musculus | 34% | 100% |
V5BSA9 | Trypanosoma cruzi | 46% | 100% |
V5DGT0 | Trypanosoma cruzi | 61% | 99% |
V5DMH3 | Trypanosoma cruzi | 26% | 100% |