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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QDE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.384 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.525 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.477 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.526 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.533 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.526 |
LIG_BIR_III_4 | 101 | 105 | PF00653 | 0.393 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.531 |
LIG_LIR_Gen_1 | 272 | 283 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.590 |
LIG_NRP_CendR_1 | 303 | 304 | PF00754 | 0.646 |
LIG_RPA_C_Fungi | 222 | 234 | PF08784 | 0.437 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.383 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.423 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.507 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.673 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.426 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.447 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.649 |
MOD_GlcNHglycan | 215 | 219 | PF01048 | 0.450 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.605 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.476 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.425 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.629 |
MOD_LATS_1 | 151 | 157 | PF00433 | 0.398 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.482 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.464 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.586 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.452 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.482 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.582 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.464 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.512 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.687 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.544 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.674 |
MOD_SUMO_rev_2 | 97 | 105 | PF00179 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.611 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIA8 | Leptomonas seymouri | 76% | 100% |
A0A1X0P7A5 | Trypanosomatidae | 37% | 97% |
A0A3Q8IB89 | Leishmania donovani | 95% | 100% |
A0A422NN36 | Trypanosoma rangeli | 35% | 100% |
A4HA29 | Leishmania braziliensis | 83% | 100% |
A4HY92 | Leishmania infantum | 95% | 100% |
D0A0M5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AS24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5B7K2 | Trypanosoma cruzi | 36% | 99% |