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 |
Related structures:
AlphaFold database: Q4QFB9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.793 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.744 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.695 |
CLV_PCSK_FUR_1 | 207 | 211 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.808 |
CLV_Separin_Metazoa | 99 | 103 | PF03568 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 113 | 119 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 292 | 302 | PF00069 | 0.708 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.694 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.706 |
DOC_PP4_MxPP_1 | 112 | 115 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 187 | 195 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 452 | 459 | PF00244 | 0.685 |
LIG_Actin_WH2_2 | 436 | 454 | PF00022 | 0.740 |
LIG_BIR_III_2 | 433 | 437 | PF00653 | 0.697 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.810 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.518 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.803 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.715 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.597 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.762 |
LIG_LIR_Apic_2 | 86 | 90 | PF02991 | 0.716 |
LIG_LIR_Gen_1 | 386 | 395 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 41 | 50 | PF02991 | 0.789 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.698 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.487 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.770 |
LIG_SH2_GRB2like | 366 | 369 | PF00017 | 0.726 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.670 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.794 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.713 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.724 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.713 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.769 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.724 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.605 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.795 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.685 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.527 |
LIG_TRAF2_1 | 475 | 478 | PF00917 | 0.683 |
LIG_WRC_WIRS_1 | 384 | 389 | PF05994 | 0.712 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.625 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.597 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.700 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.689 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.699 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.647 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.595 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.516 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.676 |
MOD_CMANNOS | 280 | 283 | PF00535 | 0.502 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.728 |
MOD_GlcNHglycan | 159 | 163 | PF01048 | 0.712 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.776 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.668 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.686 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.643 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.787 |
MOD_GlcNHglycan | 370 | 374 | PF01048 | 0.743 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.759 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.801 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.609 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.806 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.796 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.725 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.670 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.698 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.633 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.668 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.670 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.574 |
MOD_LATS_1 | 122 | 128 | PF00433 | 0.564 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.621 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.584 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.801 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.558 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.696 |
MOD_NEK2_2 | 283 | 288 | PF00069 | 0.548 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.792 |
MOD_PKA_1 | 259 | 265 | PF00069 | 0.630 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.730 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.563 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.743 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.799 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.618 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.795 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.820 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.826 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.678 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.660 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.724 |
MOD_SUMO_rev_2 | 190 | 199 | PF00179 | 0.490 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.694 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.771 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.695 |
TRG_NLS_MonoCore_2 | 288 | 293 | PF00514 | 0.670 |
TRG_NLS_MonoExtC_3 | 287 | 292 | PF00514 | 0.647 |
TRG_NLS_MonoExtN_4 | 288 | 293 | PF00514 | 0.670 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEA5 | Leptomonas seymouri | 48% | 76% |
A0A3Q8IA81 | Leishmania donovani | 94% | 100% |
A4H822 | Leishmania braziliensis | 77% | 100% |
A4HWG4 | Leishmania infantum | 94% | 100% |
E9AQ64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |