A conserved signal-anchored protein family of obscure function also found in plants and bacteria.. Some of the Leishmaniid proteins might have 3 TM segments instead of 1
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ATZ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.407 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.467 |
CLV_PCSK_PC7_1 | 458 | 464 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.320 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.544 |
DEG_APCC_KENBOX_2 | 484 | 488 | PF00400 | 0.606 |
DEG_COP1_1 | 405 | 414 | PF00400 | 0.492 |
DOC_CYCLIN_RxL_1 | 436 | 445 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 66 | 69 | PF00134 | 0.337 |
DOC_MAPK_DCC_7 | 291 | 299 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 217 | 227 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 420 | 428 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 429 | 437 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 291 | 299 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 420 | 428 | PF00069 | 0.486 |
DOC_MAPK_RevD_3 | 302 | 315 | PF00069 | 0.603 |
DOC_MAPK_RevD_3 | 449 | 463 | PF00069 | 0.584 |
DOC_PP2B_LxvP_1 | 22 | 25 | PF13499 | 0.408 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.349 |
DOC_PP2B_PxIxI_1 | 191 | 197 | PF00149 | 0.537 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.171 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.359 |
DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.621 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.219 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.174 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 510 | 514 | PF00244 | 0.515 |
LIG_CaM_IQ_9 | 147 | 163 | PF13499 | 0.537 |
LIG_eIF4E_1 | 418 | 424 | PF01652 | 0.543 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.276 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.526 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.554 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.574 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.554 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.533 |
LIG_GBD_Chelix_1 | 393 | 401 | PF00786 | 0.386 |
LIG_LIR_Apic_2 | 19 | 24 | PF02991 | 0.171 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 390 | 397 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 486 | 495 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 96 | 107 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.331 |
LIG_MYND_1 | 20 | 24 | PF01753 | 0.171 |
LIG_NRBOX | 392 | 398 | PF00104 | 0.573 |
LIG_Pex14_1 | 165 | 169 | PF04695 | 0.445 |
LIG_Pex14_1 | 391 | 395 | PF04695 | 0.472 |
LIG_RPA_C_Fungi | 167 | 179 | PF08784 | 0.414 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.364 |
LIG_SH3_2 | 478 | 483 | PF14604 | 0.566 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.273 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.364 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 184 | 189 | PF11976 | 0.270 |
LIG_SUMO_SIM_anti_2 | 448 | 455 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 89 | 97 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 192 | 198 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 501 | 507 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 89 | 97 | PF11976 | 0.580 |
LIG_WRC_WIRS_1 | 320 | 325 | PF05994 | 0.368 |
MOD_CDK_SPxK_1 | 39 | 45 | PF00069 | 0.460 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.171 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.406 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.603 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.518 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.439 |
MOD_CMANNOS | 349 | 352 | PF00535 | 0.627 |
MOD_Cter_Amidation | 273 | 276 | PF01082 | 0.469 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.450 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.592 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.451 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.607 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.565 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.489 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.364 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.389 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.452 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.443 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.493 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.412 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.371 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.474 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.533 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.576 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.405 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.339 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.447 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.419 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.171 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.409 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.381 |
MOD_PKB_1 | 219 | 227 | PF00069 | 0.339 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.223 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.445 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.469 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.214 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.285 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.546 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.483 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.527 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.561 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.441 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.219 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.520 |
MOD_SUMO_rev_2 | 149 | 156 | PF00179 | 0.394 |
TRG_DiLeu_BaEn_1 | 486 | 491 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_2 | 141 | 147 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 397 | 402 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.364 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 515 | 519 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN0 | Leptomonas seymouri | 73% | 100% |
A0A0S4J7E4 | Bodo saltans | 35% | 100% |
A0A1X0P0I4 | Trypanosomatidae | 42% | 100% |
A0A3R7R7J3 | Trypanosoma rangeli | 43% | 100% |
A0A3S7XC13 | Leishmania donovani | 89% | 100% |
A4HQ77 | Leishmania braziliensis | 87% | 100% |
A4IDX5 | Leishmania infantum | 92% | 97% |
D0A437 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q4Q0K0 | Leishmania major | 91% | 100% |
V5B3M2 | Trypanosoma cruzi | 41% | 100% |