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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8IG98
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.406 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.465 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.496 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.598 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.466 |
DOC_PP2B_LxvP_1 | 180 | 183 | PF13499 | 0.423 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.605 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.399 |
LIG_deltaCOP1_diTrp_1 | 158 | 164 | PF00928 | 0.392 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.372 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.564 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.416 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.717 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.517 |
LIG_LIR_Apic_2 | 200 | 204 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 233 | 238 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 222 | 232 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.386 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.490 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.578 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.499 |
LIG_SH3_1 | 147 | 153 | PF00018 | 0.500 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.646 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.458 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.409 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.632 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.502 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.730 |
LIG_SUMO_SIM_par_1 | 178 | 185 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 57 | 62 | PF11976 | 0.485 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.560 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.445 |
MOD_CDC14_SPxK_1 | 49 | 52 | PF00782 | 0.604 |
MOD_CDC14_SPxK_1 | 75 | 78 | PF00782 | 0.674 |
MOD_CDC14_SPxK_1 | 90 | 93 | PF00782 | 0.479 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.784 |
MOD_CDK_SPxK_1 | 72 | 78 | PF00069 | 0.676 |
MOD_CDK_SPxK_1 | 87 | 93 | PF00069 | 0.491 |
MOD_CDK_SPxxK_3 | 214 | 221 | PF00069 | 0.475 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.455 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.650 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.545 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.662 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.576 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.461 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.458 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.385 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.544 |
MOD_DYRK1A_RPxSP_1 | 78 | 82 | PF00069 | 0.635 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.595 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.274 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.662 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.671 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.693 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.383 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.738 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.675 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.523 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.658 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.411 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.574 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.536 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.603 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.444 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.465 |
MOD_PK_1 | 64 | 70 | PF00069 | 0.755 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.596 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.459 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.405 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.458 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.414 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.461 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.479 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.762 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.748 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.701 |
MOD_SUMO_rev_2 | 184 | 192 | PF00179 | 0.432 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.615 |
TRG_DiLeu_BaEn_4 | 6 | 12 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 176 | 181 | PF01217 | 0.355 |
TRG_DiLeu_LyEn_5 | 6 | 11 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 9 | 14 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT8 | Leptomonas seymouri | 56% | 95% |
A0A0S4IRN5 | Bodo saltans | 37% | 100% |
A0A3R7P3C4 | Trypanosoma rangeli | 42% | 100% |
A4HL01 | Leishmania braziliensis | 78% | 100% |
A4I8I2 | Leishmania infantum | 99% | 100% |
E9B3E2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q4R0 | Leishmania major | 94% | 100% |