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. | yes | yes: 5 |
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 | yes | yes: 7, no: 1 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4H7L3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.689 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.612 |
DOC_CYCLIN_RxL_1 | 80 | 89 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.372 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 267 | 275 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 52 | 59 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 9 | 16 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 166 | 173 | PF00149 | 0.476 |
DOC_PP1_SILK_1 | 453 | 458 | PF00149 | 0.773 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 273 | 276 | PF13499 | 0.372 |
DOC_PP2B_PxIxI_1 | 54 | 60 | PF00149 | 0.468 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.733 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.726 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.483 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.606 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 151 | 157 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 333 | 341 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 346 | 350 | PF00244 | 0.838 |
LIG_14-3-3_CanoR_1 | 424 | 429 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 458 | 465 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.777 |
LIG_BIR_III_2 | 32 | 36 | PF00653 | 0.450 |
LIG_BIR_III_4 | 218 | 222 | PF00653 | 0.544 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.696 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.692 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 114 | 120 | PF00928 | 0.423 |
LIG_EH_1 | 141 | 145 | PF12763 | 0.392 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.476 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.535 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.611 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.418 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.633 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.622 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.673 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.407 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.529 |
LIG_GBD_Chelix_1 | 283 | 291 | PF00786 | 0.356 |
LIG_LIR_Apic_2 | 347 | 352 | PF02991 | 0.758 |
LIG_LIR_Apic_2 | 476 | 480 | PF02991 | 0.729 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.446 |
LIG_NRBOX | 14 | 20 | PF00104 | 0.578 |
LIG_PDZ_Class_2 | 484 | 489 | PF00595 | 0.752 |
LIG_Pex14_1 | 116 | 120 | PF04695 | 0.498 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.481 |
LIG_Pex14_2 | 473 | 477 | PF04695 | 0.693 |
LIG_Pex14_2 | 70 | 74 | PF04695 | 0.473 |
LIG_PTB_Apo_2 | 102 | 109 | PF02174 | 0.514 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.484 |
LIG_SH2_SRC | 235 | 238 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.451 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.658 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.705 |
LIG_SH3_4 | 300 | 307 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 26 | 32 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 270 | 275 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 213 | 218 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 26 | 32 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 275 | 280 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 53 | 61 | PF11976 | 0.482 |
LIG_UBA3_1 | 119 | 127 | PF00899 | 0.411 |
LIG_UBA3_1 | 292 | 300 | PF00899 | 0.372 |
LIG_WRC_WIRS_1 | 365 | 370 | PF05994 | 0.664 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.394 |
MOD_CDK_SPK_2 | 341 | 346 | PF00069 | 0.697 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.475 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.468 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.758 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.706 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.732 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.823 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.779 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.730 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.847 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.739 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.473 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.458 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.679 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.688 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.332 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.552 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.524 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.518 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.517 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.577 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.588 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.569 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.729 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.743 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.725 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.812 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.736 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.879 |
MOD_LATS_1 | 422 | 428 | PF00433 | 0.757 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.677 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.673 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.736 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.605 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.532 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.703 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.690 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.675 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.410 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.543 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.478 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.455 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.679 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.690 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.768 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.592 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.758 |
MOD_PKA_1 | 457 | 463 | PF00069 | 0.743 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.827 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.771 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.842 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.886 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.722 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.505 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.532 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.398 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.694 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.492 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.489 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.520 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.563 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.482 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.280 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.714 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.811 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.762 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.465 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.459 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.457 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.524 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.440 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.458 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.694 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.694 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.680 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.497 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.759 |
MOD_SUMO_for_1 | 303 | 306 | PF00179 | 0.744 |
MOD_SUMO_rev_2 | 318 | 328 | PF00179 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 477 | 482 | PF01217 | 0.725 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.574 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.716 |
TRG_NLS_MonoCore_2 | 329 | 334 | PF00514 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W9 | Leptomonas seymouri | 35% | 100% |
A0A3Q8I9R5 | Leishmania donovani | 28% | 100% |
A0A3S7WSX8 | Leishmania donovani | 71% | 100% |
A4HVZ7 | Leishmania infantum | 28% | 100% |
A4HVZ8 | Leishmania infantum | 71% | 100% |
E9APQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QFS9 | Leishmania major | 67% | 94% |