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: 9 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 52 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 69 |
NetGPI | no | yes: 0, no: 69 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 70 |
GO:0110165 | cellular anatomical entity | 1 | 70 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AJY4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015877 | biopterin transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015224 | biopterin transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.325 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.211 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.211 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.443 |
DEG_SCF_TRCP1_1 | 133 | 138 | PF00400 | 0.205 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.465 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.251 |
DOC_ANK_TNKS_1 | 12 | 19 | PF00023 | 0.485 |
DOC_CKS1_1 | 504 | 509 | PF01111 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 306 | 312 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 42 | 48 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 541 | 550 | PF00069 | 0.709 |
DOC_MAPK_MEF2A_6 | 136 | 143 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 407 | 414 | PF00069 | 0.361 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.448 |
DOC_PP2B_PxIxI_1 | 136 | 142 | PF00149 | 0.288 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.262 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.385 |
DOC_USP7_UBL2_3 | 204 | 208 | PF12436 | 0.414 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 259 | 264 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.496 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.331 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.516 |
LIG_EVH1_2 | 488 | 492 | PF00568 | 0.365 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.348 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.584 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.366 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.261 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.340 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.416 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.423 |
LIG_LIR_Gen_1 | 111 | 122 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 285 | 294 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 32 | 40 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 353 | 362 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 398 | 405 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 453 | 462 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 491 | 500 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 8 | 17 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 491 | 495 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.532 |
LIG_NRBOX | 494 | 500 | PF00104 | 0.226 |
LIG_PDZ_Class_2 | 545 | 550 | PF00595 | 0.557 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.337 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.286 |
LIG_Pex14_2 | 317 | 321 | PF04695 | 0.368 |
LIG_Pex14_2 | 350 | 354 | PF04695 | 0.316 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.379 |
LIG_Pex14_2 | 78 | 82 | PF04695 | 0.382 |
LIG_REV1ctd_RIR_1 | 173 | 182 | PF16727 | 0.384 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.519 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.359 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.315 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.309 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.384 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.331 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 326 | 329 | PF00017 | 0.355 |
LIG_SH2_PTP2 | 411 | 414 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.305 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.286 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.408 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 401 | 406 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 273 | 278 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 401 | 406 | PF11976 | 0.355 |
LIG_TYR_ITIM | 289 | 294 | PF00017 | 0.381 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.341 |
LIG_TYR_ITIM | 58 | 63 | PF00017 | 0.393 |
LIG_TYR_ITSM | 351 | 358 | PF00017 | 0.428 |
LIG_UBA3_1 | 174 | 178 | PF00899 | 0.523 |
LIG_UBA3_1 | 442 | 449 | PF00899 | 0.226 |
LIG_Vh1_VBS_1 | 275 | 293 | PF01044 | 0.468 |
LIG_WRC_WIRS_1 | 459 | 464 | PF05994 | 0.230 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.387 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.413 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.358 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.365 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.585 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.312 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.419 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.391 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.326 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.379 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.440 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.357 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.428 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.389 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.414 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.321 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.360 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.482 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.386 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.370 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.387 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.339 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.520 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.360 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.392 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.513 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.304 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.370 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.290 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.378 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.310 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.348 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.360 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.358 |
MOD_NEK2_2 | 451 | 456 | PF00069 | 0.226 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.226 |
MOD_PK_1 | 259 | 265 | PF00069 | 0.226 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.190 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.403 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.229 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.407 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.356 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.303 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.448 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.403 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.303 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.329 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.434 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.385 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.446 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.353 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.334 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.390 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.368 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.430 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.424 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.441 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.461 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.425 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 94 | 99 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 541 | 544 | PF00400 | 0.479 |
TRG_NLS_MonoExtN_4 | 204 | 210 | PF00514 | 0.188 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 45% | 78% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 82% |
A0A0N1HZ06 | Leptomonas seymouri | 38% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 41% | 77% |
A0A0N1PB77 | Leptomonas seymouri | 40% | 85% |
A0A0N1PBZ2 | Leptomonas seymouri | 45% | 82% |
A0A0N1PCC1 | Leptomonas seymouri | 44% | 82% |
A0A0S4INN8 | Bodo saltans | 31% | 85% |
A0A381MBI0 | Leishmania infantum | 93% | 83% |
A0A3Q8I8X7 | Leishmania donovani | 93% | 83% |
A0A3Q8IAZ0 | Leishmania donovani | 45% | 79% |
A0A3Q8IH50 | Leishmania donovani | 48% | 76% |
A0A3Q8IVN0 | Leishmania donovani | 39% | 88% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 86% |
A0A3S5H5P4 | Leishmania donovani | 46% | 81% |
A0A3S5H5V2 | Leishmania donovani | 45% | 84% |
A0A3S5H6F6 | Leishmania donovani | 44% | 79% |
A0A3S5H763 | Leishmania donovani | 49% | 82% |
A0A3S7WR10 | Leishmania donovani | 42% | 74% |
A0A3S7WR14 | Leishmania donovani | 47% | 80% |
A0A3S7WR24 | Leishmania donovani | 45% | 78% |
A4H4T8 | Leishmania braziliensis | 45% | 100% |
A4H5Y4 | Leishmania braziliensis | 85% | 100% |
A4H617 | Leishmania braziliensis | 46% | 100% |
A4H618 | Leishmania braziliensis | 46% | 100% |
A4H619 | Leishmania braziliensis | 47% | 100% |
A4H620 | Leishmania braziliensis | 51% | 100% |
A4H6C3 | Leishmania braziliensis | 83% | 100% |
A4HNH7 | Leishmania braziliensis | 40% | 100% |
A4HSS2 | Leishmania infantum | 46% | 81% |
A4HUE4 | Leishmania infantum | 42% | 74% |
A4HUE5 | Leishmania infantum | 46% | 80% |
A4HUE6 | Leishmania infantum | 47% | 80% |
A4HUE7 | Leishmania infantum | 45% | 79% |
A4HUE8 | Leishmania infantum | 45% | 78% |
A4HUF4 | Leishmania infantum | 44% | 79% |
A4HUF5 | Leishmania infantum | 48% | 84% |
A4HYA9 | Leishmania infantum | 49% | 82% |
A4IC33 | Leishmania infantum | 39% | 87% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 84% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 84% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 87% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 87% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 87% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 86% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AG72 | Leishmania infantum | 45% | 84% |
E9AI40 | Leishmania braziliensis | 46% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 81% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 84% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 74% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 84% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 91% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 77% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 83% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 82% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 87% |
Q4QDC4 | Leishmania major | 48% | 100% |
Q4QH81 | Leishmania major | 93% | 100% |
Q4QHH7 | Leishmania major | 46% | 100% |
Q4QHH8 | Leishmania major | 44% | 100% |
Q4QHH9 | Leishmania major | 44% | 100% |
Q4QHI0 | Leishmania major | 44% | 100% |
Q4QHI1 | Leishmania major | 46% | 100% |
Q4QHI2 | Leishmania major | 45% | 100% |
Q4QIU9 | Leishmania major | 45% | 100% |
Q4QJ48 | Leishmania major | 45% | 100% |
Q7KIP2 | Leishmania major | 39% | 100% |