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: Q4Q3L1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.821 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.793 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.676 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 39 | 41 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.618 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.836 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.613 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.782 |
DOC_MAPK_gen_1 | 108 | 116 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 108 | 116 | PF00069 | 0.565 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.839 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.662 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 27 | 31 | PF12436 | 0.561 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.619 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.818 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.811 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.671 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.477 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.666 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.659 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.608 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.702 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.705 |
LIG_PDZ_Class_2 | 349 | 354 | PF00595 | 0.748 |
LIG_SH3_2 | 233 | 238 | PF14604 | 0.782 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.702 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.691 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.687 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.594 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.633 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.799 |
LIG_TRAF2_1 | 5 | 8 | PF00917 | 0.506 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.781 |
MOD_CDK_SPxK_1 | 172 | 178 | PF00069 | 0.585 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.781 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.783 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.825 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.668 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.599 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.771 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.717 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.759 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.752 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.561 |
MOD_GlcNHglycan | 274 | 278 | PF01048 | 0.599 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.705 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.800 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.707 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.491 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.817 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.586 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.700 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.800 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.789 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.732 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.655 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.766 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.683 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.668 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.535 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.594 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.763 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.755 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.443 |
MOD_PKA_1 | 231 | 237 | PF00069 | 0.741 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.825 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.738 |
MOD_PKB_1 | 239 | 247 | PF00069 | 0.749 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.607 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.770 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.781 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.819 |
MOD_SUMO_for_1 | 75 | 78 | PF00179 | 0.549 |
MOD_SUMO_for_1 | 79 | 82 | PF00179 | 0.485 |
MOD_SUMO_for_1 | 85 | 88 | PF00179 | 0.499 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 165 | 173 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 7 | 11 | PF00179 | 0.507 |
TRG_DiLeu_BaEn_1 | 141 | 146 | PF01217 | 0.620 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.709 |
TRG_NLS_Bipartite_1 | 39 | 56 | PF00514 | 0.605 |
TRG_NLS_MonoExtN_4 | 51 | 56 | PF00514 | 0.665 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IUB2 | Leishmania donovani | 88% | 77% |
A4HM33 | Leishmania braziliensis | 54% | 100% |
A4I9G6 | Leishmania infantum | 88% | 77% |
E9B4G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 92% |