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: Q4QBJ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.718 |
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.734 |
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.587 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.607 |
CLV_Separin_Metazoa | 287 | 291 | PF03568 | 0.538 |
DEG_COP1_1 | 263 | 272 | PF00400 | 0.492 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.507 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.594 |
DOC_CYCLIN_RxL_1 | 139 | 152 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.534 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.608 |
DOC_PP2B_LxvP_1 | 315 | 318 | PF13499 | 0.495 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.569 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.691 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 18 | 25 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 282 | 289 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 42 | 49 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.466 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.664 |
LIG_EH_1 | 178 | 182 | PF12763 | 0.452 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.542 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.630 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.742 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.671 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.707 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.479 |
LIG_LIR_Apic_2 | 12 | 16 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 231 | 239 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.559 |
LIG_PDZ_Class_2 | 360 | 365 | PF00595 | 0.659 |
LIG_SH2_NCK_1 | 350 | 354 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.622 |
LIG_SUMO_SIM_par_1 | 265 | 271 | PF11976 | 0.493 |
LIG_TRAF2_1 | 135 | 138 | PF00917 | 0.507 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.521 |
LIG_UBA3_1 | 169 | 177 | PF00899 | 0.571 |
LIG_WRC_WIRS_1 | 234 | 239 | PF05994 | 0.588 |
MOD_CDC14_SPxK_1 | 71 | 74 | PF00782 | 0.504 |
MOD_CDK_SPxK_1 | 68 | 74 | PF00069 | 0.507 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.458 |
MOD_CDK_SPxxK_3 | 68 | 75 | PF00069 | 0.645 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.585 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.675 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.618 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.652 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.465 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.651 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.440 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.654 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.575 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.614 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.587 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.573 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.531 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.713 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.633 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.610 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.550 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.739 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.481 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.608 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.540 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.629 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.584 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.598 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.664 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.689 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.610 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.572 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.601 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.718 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.588 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.633 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.612 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.588 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.680 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.473 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.558 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.474 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.588 |
MOD_Plk_2-3 | 227 | 233 | PF00069 | 0.584 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.608 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.571 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.726 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.709 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.611 |
TRG_DiLeu_BaEn_2 | 232 | 238 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 3 | 8 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.521 |
TRG_NLS_MonoExtC_3 | 58 | 63 | PF00514 | 0.718 |
TRG_NLS_MonoExtN_4 | 59 | 64 | PF00514 | 0.730 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4X3 | Leptomonas seymouri | 40% | 97% |
A0A1X0NTI1 | Trypanosomatidae | 32% | 100% |
A0A3Q8IAT9 | Leishmania donovani | 91% | 100% |
A0A422N4X5 | Trypanosoma rangeli | 31% | 100% |
A4HCJ6 | Leishmania braziliensis | 71% | 97% |
A4I016 | Leishmania infantum | 91% | 100% |
C9ZQ77 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AVY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5ARZ4 | Trypanosoma cruzi | 31% | 100% |