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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HCG8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.819 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.753 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.641 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.569 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.814 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 173 | 177 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.405 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.601 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.690 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.643 |
LIG_LIR_Gen_1 | 120 | 125 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.668 |
LIG_PCNA_yPIPBox_3 | 387 | 401 | PF02747 | 0.730 |
LIG_REV1ctd_RIR_1 | 47 | 52 | PF16727 | 0.511 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.392 |
LIG_SH2_STAT3 | 8 | 11 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.502 |
LIG_SH3_2 | 75 | 80 | PF14604 | 0.578 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.608 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.546 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.723 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.672 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.717 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.439 |
MOD_CDC14_SPxK_1 | 299 | 302 | PF00782 | 0.556 |
MOD_CDK_SPK_2 | 69 | 74 | PF00069 | 0.578 |
MOD_CDK_SPxK_1 | 296 | 302 | PF00069 | 0.535 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.732 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.692 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.604 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.597 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.783 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.783 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.681 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.502 |
MOD_Cter_Amidation | 15 | 18 | PF01082 | 0.597 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.628 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.737 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.711 |
MOD_GlcNHglycan | 164 | 168 | PF01048 | 0.745 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.737 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.619 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.783 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.783 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.756 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.642 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.595 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.584 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.573 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.669 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.578 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.518 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.543 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.732 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.645 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.578 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.446 |
MOD_PKA_1 | 172 | 178 | PF00069 | 0.731 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.819 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.731 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.405 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.811 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.806 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.613 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.529 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.791 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.447 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.449 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.680 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.736 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.704 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.675 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.515 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.362 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.780 |
TRG_NLS_MonoCore_2 | 170 | 175 | PF00514 | 0.491 |
TRG_NLS_MonoExtN_4 | 171 | 176 | PF00514 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.724 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P808 | Leptomonas seymouri | 47% | 100% |
A0A3Q8ICB1 | Leishmania donovani | 76% | 100% |
C9ZSP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AGZ7 | Leishmania infantum | 76% | 100% |
E9AVV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 75% |
Q4QBM0 | Leishmania major | 76% | 100% |