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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HGW0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.779 |
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.808 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.570 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.804 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.633 |
CLV_PCSK_PC7_1 | 121 | 127 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 205 | 209 | PF03568 | 0.510 |
DEG_SCF_SKP2-CKS1_1 | 70 | 77 | PF00560 | 0.769 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.527 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.498 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.611 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.523 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.705 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 50 | 55 | PF00244 | 0.490 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.492 |
LIG_EVH1_1 | 115 | 119 | PF00568 | 0.528 |
LIG_EVH1_2 | 118 | 122 | PF00568 | 0.539 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.648 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.371 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.729 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.679 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.718 |
LIG_LIR_Gen_1 | 187 | 194 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.440 |
LIG_PDZ_Class_2 | 221 | 226 | PF00595 | 0.644 |
LIG_PDZ_Wminus1_1 | 224 | 226 | PF00595 | 0.679 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.613 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.613 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 12 | 16 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.495 |
LIG_SH3_2 | 116 | 121 | PF14604 | 0.536 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.678 |
LIG_SH3_CIN85_PxpxPR_1 | 87 | 92 | PF14604 | 0.528 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.541 |
LIG_TYR_ITSM | 185 | 192 | PF00017 | 0.367 |
LIG_UBA3_1 | 56 | 63 | PF00899 | 0.517 |
LIG_WRC_WIRS_1 | 6 | 11 | PF05994 | 0.475 |
MOD_CDK_SPK_2 | 22 | 27 | PF00069 | 0.728 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.768 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.733 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.716 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.684 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.542 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.744 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.466 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.767 |
MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.545 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.799 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.754 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.626 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.481 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.715 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.719 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.638 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.672 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.362 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.613 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.603 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.496 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.435 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.520 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.419 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.557 |
MOD_PK_1 | 50 | 56 | PF00069 | 0.402 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.587 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.552 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.587 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.546 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.574 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.361 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.546 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.641 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.448 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.536 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.527 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.727 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.520 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.573 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.707 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 91 | 94 | PF00400 | 0.535 |
TRG_NLS_MonoExtC_3 | 91 | 96 | PF00514 | 0.628 |
TRG_NLS_MonoExtN_4 | 91 | 96 | PF00514 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P417 | Leptomonas seymouri | 45% | 100% |
A0A3S7X1X0 | Leishmania donovani | 70% | 100% |
A4I3Z0 | Leishmania infantum | 71% | 100% |
E9B080 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q805 | Leishmania major | 69% | 100% |