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: E9AKS4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.651 |
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.565 |
CLV_Separin_Metazoa | 195 | 199 | PF03568 | 0.560 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 264 | 268 | PF00917 | 0.611 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.609 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.603 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.499 |
DOC_ANK_TNKS_1 | 352 | 359 | PF00023 | 0.494 |
DOC_CYCLIN_yClb1_LxF_4 | 256 | 261 | PF00134 | 0.541 |
DOC_MAPK_DCC_7 | 337 | 346 | PF00069 | 0.613 |
DOC_MAPK_DCC_7 | 444 | 454 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 113 | 123 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 443 | 449 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 219 | 226 | PF00069 | 0.675 |
DOC_MAPK_MEF2A_6 | 337 | 346 | PF00069 | 0.613 |
DOC_MAPK_NFAT4_5 | 219 | 227 | PF00069 | 0.674 |
DOC_MAPK_RevD_3 | 200 | 214 | PF00069 | 0.503 |
DOC_MAPK_RevD_3 | 233 | 248 | PF00069 | 0.481 |
DOC_PP1_RVXF_1 | 256 | 262 | PF00149 | 0.544 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.656 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.587 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.679 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.605 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.651 |
LIG_CSL_BTD_1 | 200 | 203 | PF09270 | 0.542 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.617 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.636 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.569 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.555 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.633 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.521 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.545 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.627 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.616 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.565 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 75 | 82 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.648 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.475 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.628 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.645 |
LIG_SH2_GRB2like | 126 | 129 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 409 | 413 | PF00017 | 0.475 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.645 |
LIG_SH2_SRC | 310 | 313 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.685 |
LIG_SH3_1 | 329 | 335 | PF00018 | 0.572 |
LIG_SH3_2 | 332 | 337 | PF14604 | 0.572 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.628 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.619 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.599 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.577 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.699 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.487 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.564 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.599 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.611 |
MOD_CDC14_SPxK_1 | 268 | 271 | PF00782 | 0.667 |
MOD_CDK_SPxK_1 | 265 | 271 | PF00069 | 0.665 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.642 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.705 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.612 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.646 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.726 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.624 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.678 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.620 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.671 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.546 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.594 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.762 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.571 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.615 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.703 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.594 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.660 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.618 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.643 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.589 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.532 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.608 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.759 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.609 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.518 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.712 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.664 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.753 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.709 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.643 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.594 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.683 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.664 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.675 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.597 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.612 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.639 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.630 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.622 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.613 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.664 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.585 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.641 |
MOD_PK_1 | 443 | 449 | PF00069 | 0.548 |
MOD_PK_1 | 6 | 12 | PF00069 | 0.645 |
MOD_PKA_1 | 443 | 449 | PF00069 | 0.476 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.645 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.647 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.643 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.524 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.645 |
MOD_PKB_1 | 396 | 404 | PF00069 | 0.528 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.560 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.642 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.614 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.614 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.580 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.612 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.681 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.702 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.612 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.629 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.642 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 329 | 332 | PF00400 | 0.767 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3T5 | Leptomonas seymouri | 37% | 92% |
A0A3S5H5Q5 | Leishmania donovani | 81% | 100% |
A4H4L1 | Leishmania braziliensis | 54% | 100% |
A4HST7 | Leishmania infantum | 81% | 100% |
Q4QJ33 | Leishmania major | 79% | 100% |