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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q9L2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 47 | 51 | PF00656 | 0.366 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 526 | 528 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 526 | 528 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.701 |
CLV_Separin_Metazoa | 372 | 376 | PF03568 | 0.441 |
DEG_COP1_1 | 250 | 260 | PF00400 | 0.404 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.433 |
DOC_ANK_TNKS_1 | 322 | 329 | PF00023 | 0.407 |
DOC_CYCLIN_RxL_1 | 151 | 160 | PF00134 | 0.354 |
DOC_CYCLIN_RxL_1 | 303 | 312 | PF00134 | 0.375 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 209 | PF00134 | 0.520 |
DOC_MAPK_DCC_7 | 203 | 212 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 152 | 159 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 437 | 443 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.471 |
DOC_MAPK_RevD_3 | 504 | 517 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 364 | 370 | PF00149 | 0.459 |
DOC_PP2B_LxvP_1 | 206 | 209 | PF13499 | 0.555 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.404 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 19 | 29 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 332 | 337 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 366 | 370 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 375 | 384 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 399 | 406 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 437 | 442 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 469 | 478 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 360 | 377 | PF00022 | 0.453 |
LIG_BIR_III_2 | 403 | 407 | PF00653 | 0.441 |
LIG_DLG_GKlike_1 | 332 | 339 | PF00625 | 0.380 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.472 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.279 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.453 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.353 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.363 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.387 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.451 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.351 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.471 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.454 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.477 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.328 |
LIG_LIR_Apic_2 | 34 | 38 | PF02991 | 0.480 |
LIG_LIR_Apic_2 | 472 | 478 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 418 | 426 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.341 |
LIG_LYPXL_S_1 | 125 | 129 | PF13949 | 0.604 |
LIG_LYPXL_yS_3 | 126 | 129 | PF13949 | 0.405 |
LIG_NRBOX | 48 | 54 | PF00104 | 0.389 |
LIG_PCNA_yPIPBox_3 | 133 | 147 | PF02747 | 0.383 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.450 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.466 |
LIG_SH3_2 | 453 | 458 | PF14604 | 0.440 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.487 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.502 |
LIG_Sin3_3 | 168 | 175 | PF02671 | 0.390 |
LIG_SUMO_SIM_par_1 | 312 | 318 | PF11976 | 0.474 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.538 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.404 |
LIG_WRC_WIRS_1 | 421 | 426 | PF05994 | 0.469 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.399 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.456 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.519 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.434 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.452 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.373 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.532 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.371 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.468 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.426 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.557 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.591 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.503 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.619 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.684 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.602 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.740 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.631 |
MOD_GlcNHglycan | 497 | 501 | PF01048 | 0.453 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.628 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.391 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.486 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.455 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.399 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.456 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.438 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.515 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.680 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.570 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.441 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.386 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.482 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.392 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.423 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.466 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.360 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.474 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.335 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.528 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.231 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.509 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.383 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.473 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.562 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.428 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.404 |
MOD_PKA_1 | 399 | 405 | PF00069 | 0.563 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.484 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.503 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.420 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.346 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.389 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.438 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.433 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.564 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.441 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.569 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.418 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.465 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.359 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.479 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.400 |
MOD_Plk_1 | 384 | 390 | PF00069 | 0.509 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.365 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.510 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.438 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.511 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.484 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.485 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.467 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.374 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.299 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.512 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.374 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.367 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.546 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.424 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 310 | 315 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.725 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD48 | Leptomonas seymouri | 36% | 100% |
A0A3S7WZJ8 | Leishmania donovani | 91% | 100% |
A4HEC9 | Leishmania braziliensis | 72% | 99% |
A4I1S4 | Leishmania infantum | 91% | 100% |
E9AXV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 95% |