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: Q4QB27
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.712 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.619 |
CLV_PCSK_PC7_1 | 34 | 40 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.671 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.711 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.702 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.629 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.581 |
DOC_CYCLIN_RxL_1 | 152 | 164 | PF00134 | 0.621 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.715 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.639 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.562 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.663 |
LIG_Clathr_ClatBox_1 | 159 | 163 | PF01394 | 0.537 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.642 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.562 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.548 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.548 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.500 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.520 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.559 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.522 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.582 |
LIG_SH3_2 | 213 | 218 | PF14604 | 0.715 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.705 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.719 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.703 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.620 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.478 |
MOD_CDK_SPK_2 | 33 | 38 | PF00069 | 0.580 |
MOD_CDK_SPxK_1 | 212 | 218 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 33 | 39 | PF00069 | 0.584 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.743 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.672 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.744 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.657 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.632 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.590 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.566 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.507 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.541 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.652 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.569 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.562 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.691 |
MOD_GlcNHglycan | 204 | 208 | PF01048 | 0.721 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.604 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.778 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.777 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.658 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.519 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.653 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.662 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.630 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.689 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.637 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.772 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.745 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.517 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.636 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.659 |
MOD_PK_1 | 12 | 18 | PF00069 | 0.711 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.695 |
MOD_PKB_1 | 189 | 197 | PF00069 | 0.713 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.517 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.583 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.617 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.506 |
TRG_NLS_Bipartite_1 | 178 | 193 | PF00514 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4W9 | Leptomonas seymouri | 48% | 100% |
A0A3S7WXU2 | Leishmania donovani | 91% | 100% |
A4HCZ8 | Leishmania braziliensis | 70% | 100% |
A4I0I3 | Leishmania infantum | 91% | 100% |
E9AWE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |