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: E9ATK0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.813 |
CLV_PCSK_FUR_1 | 110 | 114 | PF00082 | 0.647 |
CLV_PCSK_FUR_1 | 220 | 224 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.749 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.780 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.689 |
DEG_SPOP_SBC_1 | 198 | 202 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.647 |
DOC_USP7_UBL2_3 | 87 | 91 | PF12436 | 0.683 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 23 | 28 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 306 | 313 | PF00244 | 0.651 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.734 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.570 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.713 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.739 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.557 |
LIG_SH2_NCK_1 | 291 | 295 | PF00017 | 0.614 |
LIG_SH2_SRC | 238 | 241 | PF00017 | 0.570 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.636 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.697 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.677 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.654 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.604 |
MOD_CDC14_SPxK_1 | 106 | 109 | PF00782 | 0.652 |
MOD_CDK_SPxK_1 | 103 | 109 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.651 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.698 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.599 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.640 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.713 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.793 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.715 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.647 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.632 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.619 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.814 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.603 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.535 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.711 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.638 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.500 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.613 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.734 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.648 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.625 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.512 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.597 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.714 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.665 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.646 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.663 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.805 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.780 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.727 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.465 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.563 |
MOD_NEK2_2 | 86 | 91 | PF00069 | 0.719 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.635 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.651 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.734 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.684 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.707 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.638 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.612 |
MOD_PKB_1 | 21 | 29 | PF00069 | 0.734 |
MOD_PKB_1 | 252 | 260 | PF00069 | 0.648 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.532 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.693 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.689 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.624 |
TRG_DiLeu_BaEn_4 | 151 | 157 | PF01217 | 0.652 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.718 |
TRG_NLS_Bipartite_1 | 5 | 25 | PF00514 | 0.808 |
TRG_NLS_Bipartite_1 | 91 | 113 | PF00514 | 0.746 |
TRG_NLS_MonoCore_2 | 19 | 24 | PF00514 | 0.651 |
TRG_NLS_MonoExtC_3 | 108 | 113 | PF00514 | 0.652 |
TRG_NLS_MonoExtN_4 | 107 | 113 | PF00514 | 0.649 |
TRG_NLS_MonoExtN_4 | 20 | 25 | PF00514 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.818 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3X1 | Leptomonas seymouri | 44% | 91% |
A0A3Q8IIX5 | Leishmania donovani | 83% | 100% |
A4HPT5 | Leishmania braziliensis | 58% | 97% |
A4IE57 | Leishmania infantum | 82% | 100% |
Q4Q0Z8 | Leishmania major | 82% | 98% |