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: A0A3S7WZA0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.627 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 162 | 168 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 143 | 151 | PF00400 | 0.468 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.600 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 167 | 176 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.352 |
LIG_deltaCOP1_diTrp_1 | 254 | 258 | PF00928 | 0.363 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.411 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.596 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.492 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.559 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.651 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.575 |
LIG_IRF3_LxIS_1 | 258 | 264 | PF10401 | 0.481 |
LIG_LIR_Apic_2 | 202 | 207 | PF02991 | 0.516 |
LIG_LIR_Apic_2 | 50 | 55 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 254 | 263 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 33 | 44 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.650 |
LIG_LYPXL_yS_3 | 274 | 277 | PF13949 | 0.544 |
LIG_MAD2 | 138 | 146 | PF02301 | 0.515 |
LIG_MYND_1 | 106 | 110 | PF01753 | 0.521 |
LIG_MYND_3 | 198 | 202 | PF01753 | 0.498 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.372 |
LIG_REV1ctd_RIR_1 | 287 | 297 | PF16727 | 0.492 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.330 |
LIG_SH3_1 | 12 | 18 | PF00018 | 0.506 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.665 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.515 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.530 |
LIG_SUMO_SIM_par_1 | 109 | 114 | PF11976 | 0.500 |
LIG_TRAF2_1 | 146 | 149 | PF00917 | 0.497 |
LIG_WRC_WIRS_1 | 35 | 40 | PF05994 | 0.526 |
MOD_CDK_SPxxK_3 | 130 | 137 | PF00069 | 0.390 |
MOD_CDK_SPxxK_3 | 84 | 91 | PF00069 | 0.596 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.388 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.666 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.580 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.770 |
MOD_DYRK1A_RPxSP_1 | 130 | 134 | PF00069 | 0.419 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.668 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.570 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.666 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.540 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.508 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.629 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.512 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.658 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.567 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.434 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.557 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.490 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.455 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.702 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.521 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.519 |
MOD_PK_1 | 91 | 97 | PF00069 | 0.604 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.519 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.523 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.578 |
MOD_PKB_1 | 26 | 34 | PF00069 | 0.489 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.443 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.554 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.604 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.476 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.443 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.384 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.461 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.754 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.414 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.708 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.596 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.718 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.633 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.313 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.361 |
TRG_NES_CRM1_1 | 114 | 127 | PF08389 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 306 | 311 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMC8 | Leptomonas seymouri | 54% | 99% |
A0A422NGK2 | Trypanosoma rangeli | 32% | 100% |
A4HEG9 | Leishmania braziliensis | 67% | 100% |
A4I1M1 | Leishmania infantum | 100% | 100% |
C9ZK64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 98% |
E9AXQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 98% |
Q4Q9R6 | Leishmania major | 90% | 100% |
V5BHV8 | Trypanosoma cruzi | 33% | 100% |