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: E9AUH5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.444 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.406 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.472 |
DEG_SPOP_SBC_1 | 73 | 77 | PF00917 | 0.455 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.619 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 328 | 334 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 209 | 216 | PF00069 | 0.661 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.485 |
DOC_PIKK_1 | 253 | 261 | PF02985 | 0.414 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.347 |
DOC_PP1_RVXF_1 | 63 | 70 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 377 | 380 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.503 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 363 | 372 | PF00244 | 0.608 |
LIG_Actin_WH2_2 | 344 | 362 | PF00022 | 0.504 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.574 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.635 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.467 |
LIG_IRF3_LxIS_1 | 53 | 60 | PF10401 | 0.459 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.515 |
LIG_MYND_1 | 376 | 380 | PF01753 | 0.626 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.458 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 352 | 355 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.485 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.439 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.479 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.488 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.571 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.495 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.451 |
LIG_SUMO_SIM_anti_2 | 240 | 248 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 286 | 291 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.578 |
LIG_TYR_ITSM | 42 | 49 | PF00017 | 0.451 |
LIG_WRC_WIRS_1 | 84 | 89 | PF05994 | 0.370 |
MOD_CDK_SPK_2 | 384 | 389 | PF00069 | 0.704 |
MOD_CDK_SPxxK_3 | 91 | 98 | PF00069 | 0.373 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.646 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.636 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.564 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.374 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.568 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.533 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.478 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.634 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.529 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.599 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.522 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.526 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.586 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.660 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.370 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.479 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.697 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.339 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.469 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.484 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.513 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.483 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.424 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.496 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.611 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.466 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.493 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.741 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.520 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.459 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.414 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.589 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.405 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.631 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.586 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.481 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.435 |
MOD_SUMO_rev_2 | 248 | 258 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 260 | 268 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 333 | 342 | PF00179 | 0.516 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.405 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 210 | 212 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.669 |
TRG_NLS_MonoCore_2 | 208 | 213 | PF00514 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWV5 | Leptomonas seymouri | 56% | 95% |
A0A3S7WVR4 | Leishmania donovani | 90% | 100% |
A4HYS0 | Leishmania infantum | 90% | 100% |
E9AI90 | Leishmania braziliensis | 77% | 100% |
Q4QD09 | Leishmania major | 90% | 100% |