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: A4IA53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.761 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.561 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.836 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.496 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.502 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.665 |
DOC_ANK_TNKS_1 | 100 | 107 | PF00023 | 0.620 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.694 |
DOC_CYCLIN_RxL_1 | 315 | 323 | PF00134 | 0.550 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 325 | 334 | PF00069 | 0.545 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.647 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.608 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 128 | 136 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 290 | 295 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 331 | 335 | PF00244 | 0.532 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.693 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.620 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.634 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.514 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.737 |
LIG_Integrin_RGD_1 | 198 | 200 | PF01839 | 0.634 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.612 |
LIG_SH3_1 | 59 | 65 | PF00018 | 0.667 |
LIG_SH3_2 | 313 | 318 | PF14604 | 0.583 |
LIG_SH3_2 | 65 | 70 | PF14604 | 0.640 |
LIG_SH3_2 | 77 | 82 | PF14604 | 0.613 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.625 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.614 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.746 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 157 | 165 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 236 | 243 | PF11976 | 0.591 |
LIG_SUMO_SIM_par_1 | 228 | 236 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 237 | 243 | PF11976 | 0.560 |
LIG_UBA3_1 | 161 | 168 | PF00899 | 0.474 |
MOD_CDK_SPK_2 | 320 | 325 | PF00069 | 0.561 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.690 |
MOD_CDK_SPxK_1 | 64 | 70 | PF00069 | 0.639 |
MOD_CDK_SPxxK_3 | 100 | 107 | PF00069 | 0.653 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.658 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.617 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.680 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.611 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.536 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.703 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.775 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.503 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.732 |
MOD_Cter_Amidation | 105 | 108 | PF01082 | 0.586 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.698 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.716 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.645 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.576 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.599 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.665 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.684 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.667 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.605 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.675 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.616 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.685 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.512 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.683 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.604 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.521 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.534 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.562 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.517 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.560 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.522 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.697 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.564 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.641 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.656 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.532 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.641 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.617 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.532 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.529 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.680 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.561 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.693 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.652 |
MOD_SUMO_rev_2 | 24 | 32 | PF00179 | 0.537 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.782 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.636 |
TRG_NLS_Bipartite_1 | 45 | 62 | PF00514 | 0.564 |
TRG_NLS_Bipartite_1 | 94 | 111 | PF00514 | 0.575 |
TRG_NLS_MonoExtC_3 | 57 | 62 | PF00514 | 0.576 |
TRG_NLS_MonoExtN_4 | 104 | 111 | PF00514 | 0.584 |
TRG_NLS_MonoExtN_4 | 316 | 322 | PF00514 | 0.558 |
TRG_NLS_MonoExtN_4 | 55 | 62 | PF00514 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7X2 | Leishmania donovani | 100% | 100% |
A4HAZ3 | Leishmania braziliensis | 53% | 99% |
E9B567 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q2R8 | Leishmania major | 87% | 100% |