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: E9AQC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.507 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.533 |
DEG_SCF_FBW7_1 | 154 | 161 | PF00400 | 0.517 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.686 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.648 |
DOC_CYCLIN_RxL_1 | 62 | 72 | PF00134 | 0.571 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.466 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.584 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.720 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.685 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.532 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.553 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.695 |
LIG_Integrin_RGD_1 | 278 | 280 | PF01839 | 0.688 |
LIG_MYND_1 | 118 | 122 | PF01753 | 0.668 |
LIG_RPA_C_Fungi | 48 | 60 | PF08784 | 0.542 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.605 |
LIG_SH3_1 | 11 | 17 | PF00018 | 0.609 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.628 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.619 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.732 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 228 | 233 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 203 | 209 | PF11976 | 0.535 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.594 |
LIG_WW_2 | 17 | 20 | PF00397 | 0.651 |
LIG_WW_3 | 195 | 199 | PF00397 | 0.667 |
MOD_CDK_SPK_2 | 118 | 123 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.676 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.733 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.628 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.685 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.621 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.570 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.590 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.516 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.548 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.598 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.449 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.581 |
MOD_Cter_Amidation | 275 | 278 | PF01082 | 0.539 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.701 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.582 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.485 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.650 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.635 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.743 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.629 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.562 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.639 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.565 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.772 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.742 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.745 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.773 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.481 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.629 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.730 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.558 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.582 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.539 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.711 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.560 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.478 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.518 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.471 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.525 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.539 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.725 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.543 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.728 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.818 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.399 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC2 | Leptomonas seymouri | 40% | 88% |
A0A3Q8IDH2 | Leishmania donovani | 86% | 100% |
A4H899 | Leishmania braziliensis | 62% | 100% |
A4HWM1 | Leishmania infantum | 85% | 100% |
Q4QF47 | Leishmania major | 84% | 100% |