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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AUM9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.625 |
CLV_MEL_PAP_1 | 30 | 36 | PF00089 | 0.422 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.481 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.695 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.649 |
DOC_ANK_TNKS_1 | 183 | 190 | PF00023 | 0.552 |
DOC_MAPK_gen_1 | 229 | 239 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 232 | 241 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 55 | 62 | PF00069 | 0.521 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 108 | 112 | PF12436 | 0.348 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 31 | 40 | PF00244 | 0.492 |
LIG_CtBP_PxDLS_1 | 189 | 194 | PF00389 | 0.514 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.534 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.790 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.419 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.574 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.319 |
LIG_LIR_Gen_1 | 26 | 34 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.523 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.530 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.512 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 58 | 65 | PF11976 | 0.497 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.464 |
MOD_CDC14_SPxK_1 | 169 | 172 | PF00782 | 0.648 |
MOD_CDK_SPK_2 | 107 | 112 | PF00069 | 0.354 |
MOD_CDK_SPxK_1 | 166 | 172 | PF00069 | 0.648 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.535 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.614 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.735 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.537 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.678 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.488 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.504 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.682 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.621 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.322 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.510 |
MOD_Cter_Amidation | 230 | 233 | PF01082 | 0.510 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.709 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.564 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.755 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.635 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.535 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.689 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.663 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.568 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.659 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.716 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.574 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.477 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.526 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.667 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.575 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.413 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.663 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.553 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.472 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.588 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.437 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.486 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.447 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.534 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.495 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.535 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.648 |
MOD_SUMO_for_1 | 83 | 86 | PF00179 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.550 |
TRG_NLS_MonoExtN_4 | 229 | 236 | PF00514 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBK6 | Leishmania donovani | 78% | 95% |
A4HYT3 | Leishmania infantum | 78% | 95% |
E9AIE2 | Leishmania braziliensis | 62% | 95% |
Q4QCV5 | Leishmania major | 77% | 100% |