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 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q0K0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.505 |
CLV_PCSK_PC7_1 | 150 | 156 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 478 | 484 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 439 | 447 | PF00400 | 0.574 |
DEG_APCC_KENBOX_2 | 504 | 508 | PF00400 | 0.684 |
DEG_COP1_1 | 425 | 434 | PF00400 | 0.559 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.538 |
DOC_CKS1_1 | 374 | 379 | PF01111 | 0.728 |
DOC_CKS1_1 | 60 | 65 | PF01111 | 0.328 |
DOC_CYCLIN_RxL_1 | 456 | 465 | PF00134 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 86 | 89 | PF00134 | 0.366 |
DOC_MAPK_DCC_7 | 311 | 319 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 237 | 247 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 440 | 448 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 449 | 457 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 311 | 319 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 440 | 448 | PF00069 | 0.522 |
DOC_MAPK_RevD_3 | 322 | 335 | PF00069 | 0.627 |
DOC_MAPK_RevD_3 | 469 | 483 | PF00069 | 0.618 |
DOC_PP1_RVXF_1 | 24 | 30 | PF00149 | 0.360 |
DOC_PP2B_LxvP_1 | 85 | 88 | PF13499 | 0.387 |
DOC_PP2B_PxIxI_1 | 211 | 217 | PF00149 | 0.562 |
DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.533 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 477 | 481 | PF12436 | 0.655 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.705 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.378 |
LIG_14-3-3_CanoR_1 | 296 | 300 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.333 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.189 |
LIG_CaM_IQ_9 | 167 | 183 | PF13499 | 0.562 |
LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.573 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.334 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.619 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.571 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.561 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.427 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.593 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.571 |
LIG_GBD_Chelix_1 | 413 | 421 | PF00786 | 0.407 |
LIG_LIR_Apic_2 | 64 | 69 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 244 | 255 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.182 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 410 | 417 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 506 | 515 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.189 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.330 |
LIG_LYPXL_yS_3 | 82 | 85 | PF13949 | 0.327 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.598 |
LIG_Pex14_1 | 185 | 189 | PF04695 | 0.487 |
LIG_Pex14_1 | 411 | 415 | PF04695 | 0.514 |
LIG_Pex14_1 | 74 | 78 | PF04695 | 0.330 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.167 |
LIG_RPA_C_Fungi | 187 | 199 | PF08784 | 0.448 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.434 |
LIG_SH2_PTP2 | 119 | 122 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.546 |
LIG_SH3_2 | 498 | 503 | PF14604 | 0.580 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.413 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.648 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.664 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.471 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 204 | 209 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 34 | 39 | PF11976 | 0.167 |
LIG_SUMO_SIM_anti_2 | 468 | 475 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 314 | 320 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 521 | 527 | PF11976 | 0.410 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.429 |
MOD_CDK_SPxK_1 | 59 | 65 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 373 | 380 | PF00069 | 0.483 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.640 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.530 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.456 |
MOD_CMANNOS | 369 | 372 | PF00535 | 0.658 |
MOD_Cter_Amidation | 293 | 296 | PF01082 | 0.473 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.606 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.498 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.482 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.605 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.384 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.608 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.473 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.413 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.441 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.496 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.473 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.203 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.453 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.422 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.521 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.594 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.624 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.473 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.473 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.445 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.548 |
MOD_PKB_1 | 239 | 247 | PF00069 | 0.473 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.471 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.536 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.221 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.357 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.592 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.535 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.544 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.652 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.470 |
MOD_SUMO_rev_2 | 169 | 176 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 506 | 511 | PF01217 | 0.572 |
TRG_DiLeu_BaEn_2 | 161 | 167 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 417 | 422 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 535 | 539 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN0 | Leptomonas seymouri | 72% | 100% |
A0A0S4J7E4 | Bodo saltans | 36% | 100% |
A0A1X0P0I4 | Trypanosomatidae | 41% | 100% |
A0A3R7R7J3 | Trypanosoma rangeli | 43% | 100% |
A0A3S7XC13 | Leishmania donovani | 92% | 100% |
A4HQ77 | Leishmania braziliensis | 85% | 100% |
A4IDX5 | Leishmania infantum | 90% | 100% |
D0A437 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ATZ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B3M2 | Trypanosoma cruzi | 41% | 100% |