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: E9AHV4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.450 |
CLV_MEL_PAP_1 | 36 | 42 | PF00089 | 0.515 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.563 |
CLV_PCSK_FUR_1 | 93 | 97 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.634 |
DEG_COP1_1 | 295 | 304 | PF00400 | 0.510 |
DOC_CKS1_1 | 248 | 253 | PF01111 | 0.656 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 376 | 384 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 26 | 32 | PF00149 | 0.431 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.590 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.566 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 95 | 102 | PF00244 | 0.631 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.612 |
LIG_CAP-Gly_1 | 497 | 503 | PF01302 | 0.524 |
LIG_Clathr_ClatBox_1 | 305 | 309 | PF01394 | 0.553 |
LIG_deltaCOP1_diTrp_1 | 121 | 127 | PF00928 | 0.559 |
LIG_deltaCOP1_diTrp_1 | 334 | 340 | PF00928 | 0.475 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.558 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.468 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.514 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.633 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.600 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.665 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.451 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.519 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 227 | 236 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 334 | 342 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.551 |
LIG_LYPXL_yS_3 | 353 | 356 | PF13949 | 0.514 |
LIG_MYND_1 | 9 | 13 | PF01753 | 0.714 |
LIG_NRBOX | 417 | 423 | PF00104 | 0.500 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.416 |
LIG_PCNA_yPIPBox_3 | 169 | 183 | PF02747 | 0.450 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.461 |
LIG_Pex14_2 | 458 | 462 | PF04695 | 0.492 |
LIG_PTAP_UEV_1 | 5 | 10 | PF05743 | 0.604 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 229 | 233 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.511 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.661 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.665 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.472 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.559 |
LIG_SUMO_SIM_anti_2 | 47 | 54 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 303 | 309 | PF11976 | 0.674 |
LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.498 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.652 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.452 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.550 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.598 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.406 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.534 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.577 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.596 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.694 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.472 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.599 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.496 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.656 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.683 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.511 |
MOD_CMANNOS | 335 | 338 | PF00535 | 0.469 |
MOD_CMANNOS | 459 | 462 | PF00535 | 0.497 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.592 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.732 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.580 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.805 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.622 |
MOD_GlcNHglycan | 397 | 402 | PF01048 | 0.588 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.604 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.488 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.506 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.633 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.579 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.608 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.454 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.677 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.589 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.597 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.593 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.681 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.506 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.488 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.620 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.679 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.447 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.555 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.567 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.487 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.557 |
MOD_NEK2_2 | 453 | 458 | PF00069 | 0.544 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.492 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.519 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.556 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.664 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.546 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.673 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.519 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.634 |
MOD_PKB_1 | 376 | 384 | PF00069 | 0.472 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.568 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.548 |
MOD_Plk_1 | 257 | 263 | PF00069 | 0.581 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.501 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.514 |
MOD_Plk_2-3 | 167 | 173 | PF00069 | 0.524 |
MOD_Plk_2-3 | 184 | 190 | PF00069 | 0.411 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.457 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.682 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.674 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.500 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.496 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.449 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.471 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.489 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.722 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.549 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.616 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 20 | 29 | PF00179 | 0.511 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.570 |
TRG_NLS_MonoExtC_3 | 36 | 42 | PF00514 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 218 | 222 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSZ3 | Leptomonas seymouri | 49% | 99% |
A0A3Q8IHZ9 | Leishmania donovani | 99% | 100% |
A4HMN5 | Leishmania braziliensis | 70% | 99% |
E9AF37 | Leishmania major | 87% | 100% |
E9B692 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |