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 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: E9B571
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.607 |
CLV_PCSK_PC7_1 | 275 | 281 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 474 | 478 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.455 |
DEG_APCC_DBOX_1 | 112 | 120 | PF00400 | 0.636 |
DEG_APCC_DBOX_1 | 274 | 282 | PF00400 | 0.434 |
DEG_APCC_DBOX_1 | 492 | 500 | PF00400 | 0.378 |
DEG_SPOP_SBC_1 | 8 | 12 | PF00917 | 0.517 |
DOC_CYCLIN_RxL_1 | 179 | 189 | PF00134 | 0.628 |
DOC_MAPK_DCC_7 | 309 | 317 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 309 | 317 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 389 | 396 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 232 | 240 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 309 | 317 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 389 | 398 | PF00069 | 0.299 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.253 |
DOC_PP1_RVXF_1 | 410 | 416 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 521 | 528 | PF00149 | 0.318 |
DOC_PP2B_PxIxI_1 | 285 | 291 | PF00149 | 0.310 |
DOC_PP2B_PxIxI_1 | 42 | 48 | PF00149 | 0.512 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.667 |
DOC_PP4_FxxP_1 | 527 | 530 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.393 |
DOC_USP7_MATH_2 | 399 | 405 | PF00917 | 0.261 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.368 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.584 |
LIG_14-3-3_CanoR_1 | 463 | 470 | PF00244 | 0.377 |
LIG_Actin_WH2_2 | 312 | 329 | PF00022 | 0.363 |
LIG_APCC_ABBA_1 | 96 | 101 | PF00400 | 0.503 |
LIG_APCC_ABBAyCdc20_2 | 523 | 529 | PF00400 | 0.221 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.507 |
LIG_CaMK_CASK_1 | 533 | 538 | PF00069 | 0.303 |
LIG_deltaCOP1_diTrp_1 | 533 | 542 | PF00928 | 0.330 |
LIG_eIF4E_1 | 470 | 476 | PF01652 | 0.310 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.298 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.428 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.569 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 524 | 530 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 131 | 138 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 414 | 421 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 454 | 465 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.415 |
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 | 0.339 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.532 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.555 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.309 |
LIG_PTB_Apo_2 | 536 | 543 | PF02174 | 0.291 |
LIG_PTB_Apo_2 | 82 | 89 | PF02174 | 0.558 |
LIG_REV1ctd_RIR_1 | 4 | 13 | PF16727 | 0.541 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.284 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.362 |
LIG_SH2_CRK | 79 | 83 | PF00017 | 0.528 |
LIG_SH2_GRB2like | 470 | 473 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 528 | 532 | PF00017 | 0.357 |
LIG_SH2_PTP2 | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.468 |
LIG_SH2_SRC | 528 | 531 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.712 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.399 |
LIG_SUMO_SIM_anti_2 | 362 | 368 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 42 | 49 | PF11976 | 0.550 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.489 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.333 |
LIG_TYR_ITSM | 199 | 206 | PF00017 | 0.527 |
LIG_UBA3_1 | 364 | 368 | PF00899 | 0.259 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.667 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.417 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.651 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.409 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.302 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.295 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.630 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.510 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.540 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.595 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.636 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.478 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.457 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.505 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.461 |
MOD_LATS_1 | 461 | 467 | PF00433 | 0.378 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.378 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.387 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.381 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.517 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.325 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.311 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.553 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.488 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.370 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.571 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.353 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.429 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.325 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.382 |
MOD_PKB_1 | 267 | 275 | PF00069 | 0.283 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.390 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.414 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.617 |
MOD_Plk_2-3 | 84 | 90 | PF00069 | 0.571 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.545 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.295 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 360 | 365 | PF01217 | 0.305 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.601 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 324 | 339 | PF08389 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 42% | 84% |
A0A0N1PB02 | Leptomonas seymouri | 73% | 84% |
A0A0S4J6C6 | Bodo saltans | 47% | 85% |
A0A1X0P9A6 | Trypanosomatidae | 57% | 81% |
A0A3Q8IHH1 | Leishmania donovani | 38% | 75% |
A0A3R7K2Y9 | Trypanosoma rangeli | 55% | 80% |
A0A3S5H668 | Leishmania donovani | 50% | 100% |
A0A3S5H669 | Leishmania donovani | 48% | 87% |
A0A3S7X835 | Leishmania donovani | 90% | 99% |
A4H5C9 | Leishmania braziliensis | 48% | 100% |
A4H5D0 | Leishmania braziliensis | 46% | 100% |
A4HAZ7 | Leishmania braziliensis | 69% | 100% |
A4HAZ9 | Leishmania braziliensis | 72% | 100% |
A4HB01 | Leishmania braziliensis | 72% | 100% |
A4HTM0 | Leishmania infantum | 50% | 100% |
A4HTM1 | Leishmania infantum | 48% | 87% |
A4IA57 | Leishmania infantum | 90% | 99% |
C6K3V8 | Leptomonas seymouri | 51% | 91% |
C6K3V9 | Leptomonas seymouri | 46% | 84% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 82% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 99% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q1U8 | Leishmania major | 39% | 100% |
Q4Q2R4 | Leishmania major | 91% | 100% |
Q4Q310 | Leishmania major | 40% | 100% |
Q4Q312 | Leishmania major | 40% | 100% |
Q4Q340 | Leishmania major | 40% | 100% |
Q4Q342 | Leishmania major | 40% | 100% |
Q4QI90 | Leishmania major | 45% | 100% |
Q4QI91 | Leishmania major | 49% | 99% |