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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AK87
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 184 | 190 | PF00089 | 0.490 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.655 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.565 |
DEG_SCF_FBW7_1 | 111 | 118 | PF00400 | 0.532 |
DEG_SCF_FBW7_1 | 236 | 243 | PF00400 | 0.665 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.552 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.544 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.535 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.580 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.621 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.507 |
DOC_MAPK_HePTP_8 | 48 | 60 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 51 | 60 | PF00069 | 0.571 |
DOC_MAPK_NFAT4_5 | 53 | 61 | PF00069 | 0.512 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 165 | 175 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 397 | 407 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.674 |
LIG_Actin_WH2_2 | 43 | 61 | PF00022 | 0.446 |
LIG_APCC_ABBA_1 | 438 | 443 | PF00400 | 0.619 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.754 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.646 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.644 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.573 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.541 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.567 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.540 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.568 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.557 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.587 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.646 |
LIG_LIR_Apic_2 | 201 | 205 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 153 | 159 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 169 | 178 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.713 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.552 |
LIG_LYPXL_yS_3 | 108 | 111 | PF13949 | 0.562 |
LIG_NRBOX | 31 | 37 | PF00104 | 0.500 |
LIG_PCNA_yPIPBox_3 | 23 | 36 | PF02747 | 0.516 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.633 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.588 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.495 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.605 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.708 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.680 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.701 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.727 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.502 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.483 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.734 |
LIG_WRC_WIRS_1 | 353 | 358 | PF05994 | 0.516 |
LIG_WW_3 | 184 | 188 | PF00397 | 0.631 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.517 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.411 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.716 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.677 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.618 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.716 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.630 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.586 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.690 |
MOD_DYRK1A_RPxSP_1 | 354 | 358 | PF00069 | 0.516 |
MOD_DYRK1A_RPxSP_1 | 457 | 461 | PF00069 | 0.539 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.514 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.528 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.576 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.616 |
MOD_GlcNHglycan | 3 | 7 | PF01048 | 0.715 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.561 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.704 |
MOD_GlcNHglycan | 369 | 375 | PF01048 | 0.669 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.585 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.500 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.538 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.710 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.610 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.590 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.525 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.449 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.715 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.575 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.666 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.724 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.667 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.689 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.628 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.544 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.569 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.507 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.500 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.478 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.495 |
MOD_PK_1 | 180 | 186 | PF00069 | 0.437 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.362 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.503 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.618 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.566 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.676 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.546 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.721 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.526 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.647 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.490 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.601 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.618 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.567 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.605 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.591 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.649 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.793 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.523 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.712 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.539 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.551 |
MOD_SUMO_rev_2 | 296 | 302 | PF00179 | 0.683 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.678 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.621 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.457 |
TRG_NLS_MonoExtC_3 | 195 | 201 | PF00514 | 0.572 |
TRG_NLS_MonoExtN_4 | 84 | 91 | PF00514 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WNX2 | Leishmania donovani | 82% | 98% |
A4H421 | Leishmania braziliensis | 61% | 100% |
A4HSA3 | Leishmania infantum | 82% | 98% |
Q9NF89 | Leishmania major | 81% | 100% |