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. | yes | 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: 70 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: Q4QHI1
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 | 182 | 184 | PF00675 | 0.372 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.460 |
DOC_CDC14_PxL_1 | 517 | 525 | PF14671 | 0.366 |
DOC_CKS1_1 | 529 | 534 | PF01111 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 534 | 540 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 168 | 178 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 183 | 191 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 430 | 438 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 44 | 50 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 559 | 567 | PF00069 | 0.733 |
DOC_MAPK_MEF2A_6 | 138 | 145 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 430 | 438 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 561 | 569 | PF00069 | 0.571 |
DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.399 |
DOC_PP2B_PxIxI_1 | 138 | 144 | PF00149 | 0.322 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.810 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.490 |
LIG_Clathr_ClatBox_1 | 176 | 180 | PF01394 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 503 | 509 | PF00928 | 0.277 |
LIG_eIF4E_1 | 517 | 523 | PF01652 | 0.265 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.625 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.604 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.391 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.293 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.452 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.605 |
LIG_GBD_Chelix_1 | 412 | 420 | PF00786 | 0.509 |
LIG_GBD_Chelix_1 | 450 | 458 | PF00786 | 0.538 |
LIG_HP1_1 | 462 | 466 | PF01393 | 0.434 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 327 | 333 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 503 | 507 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 539 | 543 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 35 | 42 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 396 | 403 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 477 | 487 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 94 | 105 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.571 |
LIG_PCNA_PIPBox_1 | 417 | 426 | PF02747 | 0.236 |
LIG_PDZ_Class_3 | 590 | 595 | PF00595 | 0.615 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.345 |
LIG_Pex14_2 | 398 | 402 | PF04695 | 0.406 |
LIG_Pex14_2 | 80 | 84 | PF04695 | 0.400 |
LIG_PTB_Apo_2 | 370 | 377 | PF02174 | 0.407 |
LIG_PTB_Apo_2 | 396 | 403 | PF02174 | 0.474 |
LIG_PTB_Phospho_1 | 370 | 376 | PF10480 | 0.440 |
LIG_Rb_pABgroove_1 | 418 | 426 | PF01858 | 0.368 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.546 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.653 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.380 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.337 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.410 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.392 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.361 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.549 |
LIG_SH2_GRB2like | 361 | 364 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 517 | 520 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.471 |
LIG_SH2_SRC | 245 | 248 | PF00017 | 0.474 |
LIG_SH2_SRC | 249 | 252 | PF00017 | 0.462 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 480 | 484 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.546 |
LIG_SH3_1 | 262 | 268 | PF00018 | 0.620 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.631 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.374 |
LIG_SUMO_SIM_anti_2 | 425 | 430 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 531 | 537 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 463 | 468 | PF11976 | 0.363 |
LIG_TRAF2_1 | 572 | 575 | PF00917 | 0.590 |
LIG_TRFH_1 | 62 | 66 | PF08558 | 0.396 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.416 |
LIG_TYR_ITSM | 375 | 382 | PF00017 | 0.439 |
LIG_UBA3_1 | 176 | 184 | PF00899 | 0.556 |
LIG_UBA3_1 | 397 | 404 | PF00899 | 0.450 |
LIG_UBA3_1 | 423 | 430 | PF00899 | 0.358 |
LIG_UBA3_1 | 60 | 68 | PF00899 | 0.393 |
LIG_Vh1_VBS_1 | 288 | 306 | PF01044 | 0.442 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.382 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.397 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.280 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.603 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.467 |
MOD_Cter_Amidation | 208 | 211 | PF01082 | 0.505 |
MOD_DYRK1A_RPxSP_1 | 352 | 356 | PF00069 | 0.450 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.406 |
MOD_GlcNHglycan | 579 | 583 | PF01048 | 0.703 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.723 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.394 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.476 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.442 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.456 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.515 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.409 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.414 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.399 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.409 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.419 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.662 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.390 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.536 |
MOD_N-GLC_2 | 365 | 367 | PF02516 | 0.234 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.445 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.411 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.407 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.333 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.397 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.317 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.401 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.372 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.390 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.488 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.379 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.503 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.411 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.494 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.369 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.408 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.381 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.366 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.390 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.429 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.498 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.241 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.380 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.416 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.416 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.509 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.365 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 549 | 558 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 172 | 178 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 518 | 523 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 529 | 534 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 85% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 88% |
A0A0N1HZ06 | Leptomonas seymouri | 36% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 41% | 83% |
A0A0N1PAY4 | Leptomonas seymouri | 47% | 68% |
A0A0N1PB77 | Leptomonas seymouri | 36% | 92% |
A0A0N1PBZ2 | Leptomonas seymouri | 71% | 88% |
A0A0N1PCC1 | Leptomonas seymouri | 44% | 89% |
A0A381MBI0 | Leishmania infantum | 46% | 90% |
A0A3Q8I8X7 | Leishmania donovani | 46% | 90% |
A0A3Q8IAZ0 | Leishmania donovani | 85% | 85% |
A0A3Q8IH50 | Leishmania donovani | 60% | 82% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 95% |
A0A3R7M4J1 | Trypanosoma rangeli | 42% | 93% |
A0A3S5H5P4 | Leishmania donovani | 44% | 88% |
A0A3S5H5V2 | Leishmania donovani | 46% | 91% |
A0A3S5H6F6 | Leishmania donovani | 84% | 85% |
A0A3S5H763 | Leishmania donovani | 56% | 88% |
A0A3S7WR10 | Leishmania donovani | 43% | 80% |
A0A3S7WR14 | Leishmania donovani | 93% | 87% |
A0A3S7WR15 | Leishmania donovani | 73% | 70% |
A0A3S7WR24 | Leishmania donovani | 85% | 85% |
A4H4T8 | Leishmania braziliensis | 43% | 91% |
A4H5Y4 | Leishmania braziliensis | 46% | 91% |
A4H617 | Leishmania braziliensis | 75% | 85% |
A4H618 | Leishmania braziliensis | 73% | 87% |
A4H619 | Leishmania braziliensis | 75% | 85% |
A4H620 | Leishmania braziliensis | 61% | 84% |
A4H6C3 | Leishmania braziliensis | 45% | 91% |
A4HNH7 | Leishmania braziliensis | 37% | 95% |
A4HSS2 | Leishmania infantum | 45% | 88% |
A4HUE4 | Leishmania infantum | 43% | 80% |
A4HUE5 | Leishmania infantum | 72% | 86% |
A4HUE6 | Leishmania infantum | 93% | 87% |
A4HUE7 | Leishmania infantum | 85% | 85% |
A4HUE8 | Leishmania infantum | 85% | 85% |
A4HUF4 | Leishmania infantum | 84% | 85% |
A4HUF5 | Leishmania infantum | 59% | 90% |
A4HYA9 | Leishmania infantum | 56% | 88% |
A4IC33 | Leishmania infantum | 36% | 94% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 91% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 91% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 94% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 94% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 94% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 93% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 85% |
E9AG72 | Leishmania infantum | 46% | 91% |
E9AI40 | Leishmania braziliensis | 74% | 88% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 88% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 91% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 80% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 91% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 84% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 90% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 89% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 94% |
Q4QDC4 | Leishmania major | 55% | 100% |
Q4QH81 | Leishmania major | 46% | 100% |
Q4QHH7 | Leishmania major | 61% | 100% |
Q4QHH8 | Leishmania major | 87% | 100% |
Q4QHH9 | Leishmania major | 87% | 100% |
Q4QHI0 | Leishmania major | 88% | 100% |
Q4QHI2 | Leishmania major | 82% | 89% |
Q4QIU9 | Leishmania major | 46% | 91% |
Q4QJ48 | Leishmania major | 45% | 88% |
Q7KIP2 | Leishmania major | 37% | 100% |