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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H3W2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.391 |
DEG_ODPH_VHL_1 | 53 | 65 | PF01847 | 0.439 |
DOC_CDC14_PxL_1 | 51 | 59 | PF14671 | 0.452 |
DOC_CYCLIN_RxL_1 | 244 | 256 | PF00134 | 0.370 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.422 |
DOC_SPAK_OSR1_1 | 97 | 101 | PF12202 | 0.510 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.609 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.546 |
LIG_APCC_ABBA_1 | 53 | 58 | PF00400 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.512 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.800 |
LIG_eIF4E_1 | 146 | 152 | PF01652 | 0.412 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.475 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.476 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.501 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.662 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.454 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.465 |
LIG_GBD_Chelix_1 | 147 | 155 | PF00786 | 0.293 |
LIG_NRBOX | 146 | 152 | PF00104 | 0.496 |
LIG_NRBOX | 250 | 256 | PF00104 | 0.416 |
LIG_PCNA_yPIPBox_3 | 244 | 255 | PF02747 | 0.508 |
LIG_PCNA_yPIPBox_3 | 83 | 96 | PF02747 | 0.407 |
LIG_PDZ_Class_1 | 355 | 360 | PF00595 | 0.358 |
LIG_Pex14_1 | 29 | 33 | PF04695 | 0.372 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.419 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.500 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 250 | 256 | PF11976 | 0.523 |
LIG_SUMO_SIM_anti_2 | 298 | 306 | PF11976 | 0.695 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.450 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.549 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.472 |
LIG_TRFH_1 | 51 | 55 | PF08558 | 0.534 |
LIG_UBA3_1 | 151 | 159 | PF00899 | 0.348 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.516 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.476 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.489 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.539 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.492 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.415 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.672 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.478 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.432 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.550 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.545 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.471 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.642 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.619 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.627 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.697 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.586 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.525 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.475 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.533 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.623 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.478 |
MOD_PKB_1 | 7 | 15 | PF00069 | 0.536 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.405 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.530 |
MOD_Plk_2-3 | 250 | 256 | PF00069 | 0.301 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.423 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 43 | 46 | PF00179 | 0.395 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_1 | 250 | 255 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0D5 | Leptomonas seymouri | 77% | 98% |
A0A0S4JCG4 | Bodo saltans | 44% | 75% |
A0A1X0NKZ6 | Trypanosomatidae | 43% | 100% |
A0A3R7R703 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H5A3 | Leishmania donovani | 92% | 100% |
A4HS36 | Leishmania infantum | 92% | 100% |
C9ZY33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AK23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O97220 | Leishmania major | 91% | 100% |
V5D9X8 | Trypanosoma cruzi | 45% | 100% |