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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: E9B542
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.755 |
CLV_PCSK_FUR_1 | 199 | 203 | PF00082 | 0.577 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 198 | 200 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.468 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.535 |
DOC_CYCLIN_yCln2_LP_2 | 129 | 135 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 164 | 170 | PF00134 | 0.428 |
DOC_MAPK_DCC_7 | 73 | 83 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 40 | 48 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 140 | 147 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 23 | 30 | PF00069 | 0.551 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.429 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.450 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.528 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 140 | 144 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 205 | 215 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.488 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.434 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.490 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.505 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.512 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.488 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.511 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.490 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.434 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.703 |
LIG_SH3_2 | 135 | 140 | PF14604 | 0.467 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.484 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 27 | 34 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 24 | 29 | PF11976 | 0.669 |
MOD_CDC14_SPxK_1 | 137 | 140 | PF00782 | 0.464 |
MOD_CDK_SPxK_1 | 134 | 140 | PF00069 | 0.467 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.501 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.574 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.650 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.552 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.542 |
MOD_Cter_Amidation | 193 | 196 | PF01082 | 0.521 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.488 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.688 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.492 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.470 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.492 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.524 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.572 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.613 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.491 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.471 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.505 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.464 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.464 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.474 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.595 |
MOD_PK_1 | 90 | 96 | PF00069 | 0.487 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.665 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.708 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.459 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.720 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.518 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.490 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.502 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.509 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.525 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.449 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.569 |
MOD_SUMO_rev_2 | 33 | 39 | PF00179 | 0.555 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.797 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.565 |
TRG_NLS_MonoCore_2 | 197 | 202 | PF00514 | 0.532 |
TRG_NLS_MonoExtC_3 | 194 | 199 | PF00514 | 0.522 |
TRG_NLS_MonoExtN_4 | 193 | 199 | PF00514 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4IA27 | Leishmania infantum | 43% | 85% |