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: A0A3S7X2X0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.711 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.721 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.763 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.751 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.794 |
DOC_PP4_MxPP_1 | 97 | 100 | PF00568 | 0.769 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.644 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.635 |
LIG_BIR_III_2 | 34 | 38 | PF00653 | 0.665 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.797 |
LIG_BRCT_BRCA1_1 | 26 | 30 | PF00533 | 0.519 |
LIG_CSL_BTD_1 | 92 | 95 | PF09270 | 0.700 |
LIG_EVH1_1 | 79 | 83 | PF00568 | 0.717 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.738 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.689 |
LIG_LIR_Apic_2 | 132 | 136 | PF02991 | 0.593 |
LIG_LYPXL_yS_3 | 64 | 67 | PF13949 | 0.666 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.678 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.729 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.765 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.743 |
LIG_SH2_STAT3 | 115 | 118 | PF00017 | 0.754 |
LIG_SH2_STAT3 | 60 | 63 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.773 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.818 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.727 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.736 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.640 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.721 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.716 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.633 |
LIG_SH3_4 | 161 | 168 | PF00018 | 0.679 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.508 |
MOD_CDK_SPK_2 | 269 | 274 | PF00069 | 0.733 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.716 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.646 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.687 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.723 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.785 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.639 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.725 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.587 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.662 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.709 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.714 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.544 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.691 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.704 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.745 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.792 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.680 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.614 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.671 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.789 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.680 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.583 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.715 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.669 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.769 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.792 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.798 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.726 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.736 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.677 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.709 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.722 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.734 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.735 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.637 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.703 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCA0 | Leptomonas seymouri | 51% | 99% |
A4HHS6 | Leishmania braziliensis | 69% | 100% |
A4I4X7 | Leishmania infantum | 100% | 100% |
E9AED1 | Leishmania major | 91% | 100% |
E9ALF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |