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: Q4Q433
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.495 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.562 |
DEG_SCF_FBW7_1 | 168 | 175 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 167 | 171 | PF00917 | 0.613 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.726 |
DOC_MAPK_gen_1 | 210 | 217 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 246 | 256 | PF00069 | 0.600 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.710 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 307 | 316 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 181 | 199 | PF00022 | 0.453 |
LIG_BIR_III_4 | 295 | 299 | PF00653 | 0.503 |
LIG_BRCT_BRCA1_1 | 174 | 178 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.638 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.561 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.389 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.513 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.553 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.725 |
LIG_LIR_Apic_2 | 313 | 318 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 23 | 31 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 59 | 65 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.502 |
LIG_MLH1_MIPbox_1 | 174 | 178 | PF16413 | 0.576 |
LIG_PCNA_yPIPBox_3 | 114 | 126 | PF02747 | 0.469 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.467 |
LIG_SH3_2 | 287 | 292 | PF14604 | 0.586 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.607 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.723 |
LIG_SUMO_SIM_par_1 | 164 | 171 | PF11976 | 0.510 |
LIG_UBA3_1 | 206 | 211 | PF00899 | 0.488 |
LIG_WRC_WIRS_1 | 11 | 16 | PF05994 | 0.394 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.479 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.447 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.403 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.434 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.528 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.597 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.392 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.528 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.407 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.608 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.485 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.722 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.479 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.654 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.531 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.501 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.718 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.540 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.381 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.640 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.559 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.475 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.698 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.717 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.459 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.704 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.675 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.571 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.420 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.515 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.580 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.711 |
MOD_NEK2_2 | 10 | 15 | PF00069 | 0.390 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.403 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.405 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.403 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.559 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.494 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.557 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.571 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.529 |
MOD_Plk_2-3 | 65 | 71 | PF00069 | 0.592 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.545 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.540 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.419 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.520 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.639 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.485 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.379 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.516 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.608 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.597 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.594 |
TRG_DiLeu_BaEn_1 | 16 | 21 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_1 | 319 | 324 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.593 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U9 | Leptomonas seymouri | 45% | 99% |
A0A3S7X6T2 | Leishmania donovani | 93% | 100% |
A4HLL5 | Leishmania braziliensis | 79% | 100% |
A4I926 | Leishmania infantum | 93% | 100% |
E9B3Z1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |