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: A0A3Q8IL67
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.584 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 50 | 56 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.590 |
DEG_APCC_DBOX_1 | 513 | 521 | PF00400 | 0.382 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.412 |
DEG_SCF_FBW7_1 | 69 | 76 | PF00400 | 0.658 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.444 |
DOC_ANK_TNKS_1 | 183 | 190 | PF00023 | 0.580 |
DOC_CKS1_1 | 70 | 75 | PF01111 | 0.660 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 31 | 40 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 407 | 413 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 49 | 59 | PF00069 | 0.579 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.493 |
DOC_PP1_RVXF_1 | 127 | 133 | PF00149 | 0.577 |
DOC_PP1_RVXF_1 | 496 | 502 | PF00149 | 0.500 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.500 |
DOC_PP2B_PxIxI_1 | 320 | 326 | PF00149 | 0.548 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.577 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.526 |
DOC_USP7_MATH_2 | 243 | 249 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.577 |
LIG_14-3-3_CanoR_1 | 304 | 311 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 429 | 433 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 462 | 471 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.636 |
LIG_BIR_III_4 | 107 | 111 | PF00653 | 0.612 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 245 | 253 | PF00928 | 0.500 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.527 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.524 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.382 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.496 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.597 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.568 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.512 |
LIG_IRF3_LxIS_1 | 15 | 22 | PF10401 | 0.477 |
LIG_LIR_Gen_1 | 226 | 236 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 537 | 542 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.453 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.635 |
LIG_PCNA_PIPBox_1 | 520 | 529 | PF02747 | 0.419 |
LIG_PDZ_Class_1 | 537 | 542 | PF00595 | 0.475 |
LIG_REV1ctd_RIR_1 | 498 | 508 | PF16727 | 0.559 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.644 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.528 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.369 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.361 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.574 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.612 |
LIG_SH3_CIN85_PxpxPR_1 | 254 | 259 | PF14604 | 0.598 |
LIG_SUMO_SIM_anti_2 | 342 | 349 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.636 |
LIG_SUMO_SIM_par_1 | 16 | 23 | PF11976 | 0.453 |
LIG_TRAF2_1 | 326 | 329 | PF00917 | 0.633 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.497 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.613 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.620 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.484 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.590 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.617 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.573 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.653 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.379 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.649 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.573 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.443 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.556 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.567 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.340 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.457 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.576 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.370 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.557 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.495 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.730 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.537 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.365 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.444 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.535 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.627 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.441 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.667 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.529 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.568 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.623 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.643 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.606 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.530 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.573 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.556 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.341 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.349 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.369 |
MOD_NEK2_2 | 361 | 366 | PF00069 | 0.464 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.559 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.593 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.544 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.614 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.437 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.560 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.609 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.531 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.671 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.588 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.573 |
MOD_SUMO_rev_2 | 22 | 27 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 336 | 341 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.583 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.543 |
TRG_NLS_MonoExtC_3 | 48 | 53 | PF00514 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 148 | 153 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 404 | 408 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXU5 | Leptomonas seymouri | 43% | 100% |
A4HKJ8 | Leishmania braziliensis | 70% | 99% |
A4I830 | Leishmania infantum | 100% | 100% |
E9B2Y8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q568 | Leishmania major | 90% | 100% |