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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H5B5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.451 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.627 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.557 |
DOC_MAPK_MEF2A_6 | 139 | 148 | PF00069 | 0.572 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.458 |
LIG_14-3-3_CanoR_1 | 109 | 116 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.511 |
LIG_Actin_WH2_2 | 112 | 128 | PF00022 | 0.618 |
LIG_APCC_ABBA_1 | 129 | 134 | PF00400 | 0.595 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.462 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.586 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.657 |
LIG_Integrin_isoDGR_2 | 264 | 266 | PF01839 | 0.540 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.407 |
LIG_PCNA_yPIPBox_3 | 240 | 253 | PF02747 | 0.640 |
LIG_SH2_NCK_1 | 49 | 53 | PF00017 | 0.541 |
LIG_SH2_SRC | 49 | 52 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 12 | 16 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.556 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.694 |
LIG_SUMO_SIM_anti_2 | 149 | 156 | PF11976 | 0.339 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.698 |
LIG_UBA3_1 | 16 | 21 | PF00899 | 0.568 |
MOD_CDK_SPK_2 | 211 | 216 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 196 | 203 | PF00069 | 0.626 |
MOD_CDK_SPxxK_3 | 211 | 218 | PF00069 | 0.482 |
MOD_CDK_SPxxK_3 | 259 | 266 | PF00069 | 0.523 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.673 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.476 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.616 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.752 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.478 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.566 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.638 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.564 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.721 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.724 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.799 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.708 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.402 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.531 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.580 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.774 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.782 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.705 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.461 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.726 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.450 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.541 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.426 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.456 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.733 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.763 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.657 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.637 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.755 |
MOD_Plk_2-3 | 112 | 118 | PF00069 | 0.437 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.507 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.542 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.678 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.458 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.692 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.677 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.459 |
TRG_DiLeu_BaEn_1 | 136 | 141 | PF01217 | 0.491 |
TRG_DiLeu_LyEn_5 | 136 | 141 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.530 |
TRG_NES_CRM1_1 | 96 | 108 | PF08389 | 0.710 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMT4 | Leptomonas seymouri | 53% | 97% |
A0A0S4J3S7 | Bodo saltans | 24% | 100% |
A0A1X0NP32 | Trypanosomatidae | 30% | 100% |
A0A3S7WQ75 | Leishmania donovani | 75% | 98% |
A0A422NB91 | Trypanosoma rangeli | 28% | 100% |
A4HTJ6 | Leishmania infantum | 75% | 98% |
C9ZPH8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AMC7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QIC1 | Leishmania major | 74% | 100% |
V5BLF3 | Trypanosoma cruzi | 27% | 100% |