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: 20 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 9, no: 1 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HME3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.679 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.729 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.470 |
DEG_MDM2_SWIB_1 | 81 | 88 | PF02201 | 0.559 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.664 |
DOC_MAPK_gen_1 | 136 | 142 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.517 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.670 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.316 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.440 |
LIG_BIR_III_2 | 105 | 109 | PF00653 | 0.445 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.579 |
LIG_EH1_1 | 3 | 11 | PF00400 | 0.386 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.724 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.383 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.579 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.559 |
LIG_GBD_Chelix_1 | 9 | 17 | PF00786 | 0.401 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 83 | 89 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.539 |
LIG_Pex14_2 | 81 | 85 | PF04695 | 0.546 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.566 |
LIG_PTB_Phospho_1 | 204 | 210 | PF10480 | 0.567 |
LIG_Rb_LxCxE_1 | 45 | 64 | PF01857 | 0.205 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.692 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 123 | 126 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.496 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.396 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.550 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.566 |
MOD_CMANNOS | 82 | 85 | PF00535 | 0.524 |
MOD_Cter_Amidation | 127 | 130 | PF01082 | 0.598 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.595 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.652 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.697 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.706 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.561 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.657 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.532 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.426 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.551 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.622 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.531 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.479 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.640 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.582 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.639 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.435 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.614 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.640 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.630 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.668 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.628 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.447 |
MOD_SUMO_for_1 | 89 | 92 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 24 | 30 | PF00179 | 0.353 |
TRG_DiLeu_BaEn_2 | 50 | 56 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 129 | 131 | PF00400 | 0.717 |
TRG_NLS_MonoExtC_3 | 97 | 103 | PF00514 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYS8 | Leptomonas seymouri | 70% | 100% |
A0A0S4IZ22 | Bodo saltans | 38% | 100% |
A0A1X0NHR2 | Trypanosomatidae | 54% | 97% |
A0A3S7X8Z2 | Leishmania donovani | 81% | 100% |
A0A422N9T4 | Trypanosoma rangeli | 47% | 95% |
A4IB15 | Leishmania infantum | 81% | 100% |
C9ZNP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
E9AEU4 | Leishmania major | 80% | 100% |
E9B600 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |