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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HL47
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.623 |
CLV_PCSK_FUR_1 | 140 | 144 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.580 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.579 |
DOC_CKS1_1 | 311 | 316 | PF01111 | 0.436 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.658 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.713 |
DOC_USP7_MATH_2 | 207 | 213 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.734 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.669 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.671 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.574 |
LIG_BIR_III_4 | 345 | 349 | PF00653 | 0.471 |
LIG_eIF4E_1 | 198 | 204 | PF01652 | 0.468 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.588 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.599 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.638 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.604 |
LIG_GSK3_LRP6_1 | 150 | 155 | PF00069 | 0.435 |
LIG_LIR_Gen_1 | 177 | 183 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.721 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.645 |
LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.722 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.660 |
LIG_SH2_PTP2 | 179 | 182 | PF00017 | 0.474 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.770 |
LIG_SH3_1 | 148 | 154 | PF00018 | 0.676 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.558 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.730 |
MOD_CDK_SPK_2 | 232 | 237 | PF00069 | 0.650 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.442 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.713 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.623 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.576 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.637 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.596 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.600 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.704 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.665 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.622 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.459 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.718 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.516 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.596 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.577 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.598 |
MOD_LATS_1 | 187 | 193 | PF00433 | 0.471 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.621 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.630 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.524 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.580 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.642 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.556 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.589 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.566 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.500 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.684 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.610 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.669 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.564 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.580 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.704 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.678 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.552 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.634 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.732 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.616 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.439 |
MOD_SUMO_for_1 | 188 | 191 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 209 | 217 | PF00179 | 0.673 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 101 | 106 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS1 | Leptomonas seymouri | 55% | 95% |
A0A3Q8IGM9 | Leishmania donovani | 81% | 100% |
A0A422NYD6 | Trypanosoma rangeli | 38% | 88% |
A4I8M6 | Leishmania infantum | 81% | 100% |
C9ZPV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 91% |
E9B3I8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q4L2 | Leishmania major | 80% | 100% |
V5BJG4 | Trypanosoma cruzi | 40% | 88% |