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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H8H8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.582 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.469 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.712 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.335 |
DOC_MAPK_gen_1 | 128 | 136 | PF00069 | 0.464 |
DOC_PP1_RVXF_1 | 1 | 8 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 65 | 72 | PF00149 | 0.500 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.551 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 167 | 176 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 80 | 85 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 285 | 300 | PF00022 | 0.554 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.614 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.441 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.626 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.588 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.554 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.548 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.476 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.438 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.418 |
LIG_LIR_Gen_1 | 79 | 88 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.435 |
LIG_Rb_LxCxE_1 | 272 | 290 | PF01857 | 0.720 |
LIG_SH2_NCK_1 | 246 | 250 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 176 | 179 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.510 |
LIG_SUMO_SIM_anti_2 | 24 | 29 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.370 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.568 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.368 |
LIG_WRC_WIRS_1 | 156 | 161 | PF05994 | 0.467 |
MOD_CDK_SPxxK_3 | 13 | 20 | PF00069 | 0.479 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.486 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.554 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.679 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.506 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.407 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.584 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.415 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.461 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.306 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.578 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.596 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.384 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.444 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.409 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.442 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.364 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.613 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.414 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.389 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.483 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.542 |
MOD_PKB_1 | 78 | 86 | PF00069 | 0.295 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.448 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.475 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.575 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.390 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.432 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.374 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.299 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.581 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.605 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.457 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.543 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.470 |
MOD_SUMO_rev_2 | 124 | 133 | PF00179 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBY5 | Leptomonas seymouri | 70% | 100% |
A0A1X0NZ39 | Trypanosomatidae | 53% | 100% |
A0A3R7MGA8 | Trypanosoma rangeli | 50% | 99% |
A0A3S5H6X2 | Leishmania donovani | 83% | 100% |
A4HWV0 | Leishmania infantum | 83% | 100% |
C9ZW37 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 98% |
E9AQL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QEW8 | Leishmania major | 81% | 100% |
V5B947 | Trypanosoma cruzi | 50% | 100% |