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: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: A4IA57
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.598 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.611 |
CLV_PCSK_PC7_1 | 275 | 281 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.432 |
DEG_APCC_DBOX_1 | 492 | 500 | PF00400 | 0.383 |
DOC_CYCLIN_RxL_1 | 179 | 189 | PF00134 | 0.655 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 228 | 238 | PF00069 | 0.288 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 311 | 319 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 389 | 398 | PF00069 | 0.296 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.249 |
DOC_PP1_RVXF_1 | 410 | 416 | PF00149 | 0.333 |
DOC_PP2B_PxIxI_1 | 285 | 291 | PF00149 | 0.306 |
DOC_PP2B_PxIxI_1 | 42 | 48 | PF00149 | 0.504 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.657 |
DOC_PP4_FxxP_1 | 527 | 530 | PF00568 | 0.310 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.388 |
DOC_USP7_MATH_2 | 399 | 405 | PF00917 | 0.254 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.605 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.369 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 463 | 470 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 480 | 490 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 491 | 499 | PF00244 | 0.324 |
LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.362 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.488 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.494 |
LIG_BIR_III_4 | 435 | 439 | PF00653 | 0.270 |
LIG_deltaCOP1_diTrp_1 | 533 | 542 | PF00928 | 0.327 |
LIG_eIF4E_1 | 470 | 476 | PF01652 | 0.309 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.398 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.299 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.423 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.567 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.420 |
LIG_LIR_Apic_2 | 524 | 530 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 414 | 421 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 454 | 465 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 373 | 378 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.530 |
LIG_NRP_CendR_1 | 558 | 559 | PF00754 | 0.595 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.556 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.309 |
LIG_PTB_Apo_2 | 536 | 543 | PF02174 | 0.288 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.550 |
LIG_REV1ctd_RIR_1 | 4 | 13 | PF16727 | 0.536 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.284 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.359 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.524 |
LIG_SH2_GRB2like | 470 | 473 | PF00017 | 0.280 |
LIG_SH2_NCK_1 | 528 | 532 | PF00017 | 0.354 |
LIG_SH2_PTP2 | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_SRC | 528 | 531 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.552 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.394 |
LIG_SUMO_SIM_anti_2 | 361 | 368 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 42 | 49 | PF11976 | 0.542 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.492 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.330 |
LIG_TYR_ITSM | 199 | 206 | PF00017 | 0.550 |
LIG_UBA3_1 | 364 | 368 | PF00899 | 0.262 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.652 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.342 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.412 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.283 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.650 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.401 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.302 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.295 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.624 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.507 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.541 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.539 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.635 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.480 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.397 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.457 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.527 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.448 |
MOD_LATS_1 | 461 | 467 | PF00433 | 0.372 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.376 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.378 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.376 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.531 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.325 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.365 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.311 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.547 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.473 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.488 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.377 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.353 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.423 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.325 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.376 |
MOD_PKB_1 | 489 | 497 | PF00069 | 0.251 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.383 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.412 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.608 |
MOD_Plk_2-3 | 84 | 90 | PF00069 | 0.562 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.531 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.576 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.545 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.297 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.562 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.306 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 489 | 492 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 557 | 559 | PF00400 | 0.392 |
TRG_NES_CRM1_1 | 324 | 339 | PF08389 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 42% | 85% |
A0A0N1PB02 | Leptomonas seymouri | 70% | 85% |
A0A0S4J6C6 | Bodo saltans | 46% | 86% |
A0A1X0P9A6 | Trypanosomatidae | 56% | 82% |
A0A3Q8IHH1 | Leishmania donovani | 39% | 77% |
A0A3R7K2Y9 | Trypanosoma rangeli | 54% | 81% |
A0A3S5H668 | Leishmania donovani | 50% | 100% |
A0A3S5H669 | Leishmania donovani | 47% | 88% |
A0A3S7X835 | Leishmania donovani | 100% | 100% |
A4H5C9 | Leishmania braziliensis | 48% | 100% |
A4H5D0 | Leishmania braziliensis | 45% | 100% |
A4HAZ7 | Leishmania braziliensis | 66% | 100% |
A4HAZ9 | Leishmania braziliensis | 69% | 100% |
A4HB01 | Leishmania braziliensis | 69% | 100% |
A4HTM0 | Leishmania infantum | 50% | 99% |
A4HTM1 | Leishmania infantum | 47% | 100% |
C6K3V8 | Leptomonas seymouri | 50% | 92% |
C6K3V9 | Leptomonas seymouri | 45% | 85% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 83% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 99% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1U8 | Leishmania major | 39% | 100% |
Q4Q2R4 | Leishmania major | 90% | 100% |
Q4Q310 | Leishmania major | 41% | 100% |
Q4Q312 | Leishmania major | 41% | 100% |
Q4Q340 | Leishmania major | 41% | 100% |
Q4Q342 | Leishmania major | 41% | 100% |
Q4QI90 | Leishmania major | 46% | 100% |
Q4QI91 | Leishmania major | 49% | 99% |