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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4QE08
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.615 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.505 |
DEG_APCC_KENBOX_2 | 49 | 53 | PF00400 | 0.512 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.559 |
DOC_ANK_TNKS_1 | 245 | 252 | PF00023 | 0.242 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.506 |
DOC_PP1_RVXF_1 | 54 | 60 | PF00149 | 0.490 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.571 |
LIG_deltaCOP1_diTrp_1 | 178 | 187 | PF00928 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 231 | 241 | PF00928 | 0.449 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.507 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.314 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.614 |
LIG_LIR_Apic_2 | 364 | 369 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 355 | 366 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.614 |
LIG_NRP_CendR_1 | 387 | 389 | PF00754 | 0.736 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.344 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.500 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.449 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.367 |
LIG_SH3_1 | 167 | 173 | PF00018 | 0.514 |
LIG_SH3_2 | 382 | 387 | PF14604 | 0.627 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.363 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.465 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.620 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 351 | 357 | PF11976 | 0.569 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.483 |
MOD_CDK_SPxK_1 | 100 | 106 | PF00069 | 0.585 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.665 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.632 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.385 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.393 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.475 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.500 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.625 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.314 |
MOD_Cter_Amidation | 244 | 247 | PF01082 | 0.242 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.733 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.399 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.413 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.413 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.660 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.618 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.672 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.723 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.448 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.614 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.415 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.145 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.653 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.572 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.708 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.744 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.782 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.570 |
MOD_OFUCOSY | 156 | 163 | PF10250 | 0.467 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.612 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.638 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.751 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.559 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.625 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.605 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.325 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.640 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.532 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.523 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.432 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.500 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.635 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 7 | 12 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P400 | Leptomonas seymouri | 60% | 92% |
A0A1X0P6R6 | Trypanosomatidae | 46% | 100% |
A0A3Q8IAW5 | Leishmania donovani | 96% | 100% |
A0A422NWL4 | Trypanosoma rangeli | 42% | 100% |
A4H9D8 | Leishmania braziliensis | 79% | 86% |
A4HXQ9 | Leishmania infantum | 96% | 100% |
B6DTF3 | Bodo saltans | 30% | 100% |
D0A041 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ARH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5DN00 | Trypanosoma cruzi | 41% | 100% |