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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AG22
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.601 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.483 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.529 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 256 | 262 | PF00134 | 0.561 |
DOC_MAPK_DCC_7 | 8 | 17 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 240 | 249 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 8 | 14 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.478 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.474 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 95 | 102 | PF00244 | 0.627 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.594 |
LIG_deltaCOP1_diTrp_1 | 203 | 211 | PF00928 | 0.485 |
LIG_EH1_1 | 225 | 233 | PF00400 | 0.457 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.530 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.473 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.375 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.378 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.495 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 16 | 21 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.594 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.594 |
LIG_MYND_3 | 12 | 16 | PF01753 | 0.560 |
LIG_PDZ_Class_3 | 263 | 268 | PF00595 | 0.657 |
LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.373 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.639 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.575 |
LIG_SUMO_SIM_par_1 | 179 | 184 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.470 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.658 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.554 |
MOD_CDC14_SPxK_1 | 193 | 196 | PF00782 | 0.517 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.596 |
MOD_CDK_SPxK_1 | 190 | 196 | PF00069 | 0.495 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.516 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.652 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.630 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.395 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.512 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.733 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.705 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.593 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.730 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.453 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.328 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.635 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.518 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.778 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.510 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.506 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.547 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.572 |
MOD_PK_1 | 227 | 233 | PF00069 | 0.341 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.646 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.608 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.462 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.534 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.648 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.437 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.458 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.341 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.497 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.548 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.553 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 42 | 45 | PF00179 | 0.748 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_2 | 15 | 21 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.598 |
TRG_NLS_MonoExtC_3 | 92 | 97 | PF00514 | 0.695 |
TRG_NLS_MonoExtN_4 | 93 | 98 | PF00514 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W5 | Leptomonas seymouri | 46% | 100% |
A0A1X0P8M5 | Trypanosomatidae | 31% | 100% |
A0A3R7KU56 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H519 | Leishmania donovani | 99% | 100% |
A4H3H5 | Leishmania braziliensis | 73% | 100% |
E9ACF0 | Leishmania major | 90% | 100% |
E9AJN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5ANT9 | Trypanosoma cruzi | 32% | 100% |