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: E9B211
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.539 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.777 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.600 |
DEG_SPOP_SBC_1 | 331 | 335 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.521 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.636 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.514 |
LIG_EVH1_2 | 93 | 97 | PF00568 | 0.501 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.772 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.654 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.538 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.671 |
LIG_Integrin_RGD_1 | 114 | 116 | PF01839 | 0.549 |
LIG_LIR_Apic_2 | 213 | 219 | PF02991 | 0.755 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.747 |
LIG_SH2_NCK_1 | 185 | 189 | PF00017 | 0.740 |
LIG_SH2_SRC | 185 | 188 | PF00017 | 0.737 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.689 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.656 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.642 |
MOD_CDC14_SPxK_1 | 65 | 68 | PF00782 | 0.508 |
MOD_CDK_SPK_2 | 135 | 140 | PF00069 | 0.521 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.507 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.635 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.684 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.739 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.727 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.717 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.625 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.705 |
MOD_Cter_Amidation | 339 | 342 | PF01082 | 0.776 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.588 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.524 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.553 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.761 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.725 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.607 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.734 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.794 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.721 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.650 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.759 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.657 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.742 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.682 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.724 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.699 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.649 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.712 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.528 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.727 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.588 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.560 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.565 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.677 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.575 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.763 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.620 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.664 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.505 |
MOD_PKA_1 | 255 | 261 | PF00069 | 0.724 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.646 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.623 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.706 |
MOD_PKB_1 | 328 | 336 | PF00069 | 0.538 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.730 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.782 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.628 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.601 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.619 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.587 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.704 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.713 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.573 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.709 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.563 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.700 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.674 |
MOD_SUMO_rev_2 | 157 | 164 | PF00179 | 0.534 |
TRG_DiLeu_BaEn_1 | 33 | 38 | PF01217 | 0.565 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.587 |
TRG_ER_diLys_1 | 339 | 344 | PF00400 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILC0 | Leptomonas seymouri | 33% | 83% |
A0A3S5H7Q3 | Leishmania donovani | 78% | 96% |
A4HJJ2 | Leishmania braziliensis | 57% | 100% |
A4I6Z0 | Leishmania infantum | 78% | 96% |
E9AEF6 | Leishmania major | 75% | 100% |