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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IDX6
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 9 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0008170 | N-methyltransferase activity | 5 | 12 |
GO:0008276 | protein methyltransferase activity | 3 | 12 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 12 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 12 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.307 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.452 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.478 |
DOC_CYCLIN_RxL_1 | 147 | 158 | PF00134 | 0.553 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.485 |
DOC_MAPK_FxFP_2 | 521 | 524 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 371 | 379 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 422 | 431 | PF00069 | 0.561 |
DOC_MAPK_RevD_3 | 63 | 78 | PF00069 | 0.554 |
DOC_PIKK_1 | 169 | 177 | PF02985 | 0.554 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.471 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 521 | 524 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.784 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.506 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.658 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.478 |
LIG_14-3-3_CanoR_1 | 147 | 156 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 234 | 242 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 220 | 236 | PF00022 | 0.486 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.680 |
LIG_BIR_III_4 | 472 | 476 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.460 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.460 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.460 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.442 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.696 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.474 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.478 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.471 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.785 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.553 |
LIG_Integrin_RGD_1 | 78 | 80 | PF01839 | 0.340 |
LIG_LIR_Apic_2 | 115 | 119 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 483 | 488 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 518 | 524 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.460 |
LIG_LYPXL_S_1 | 187 | 191 | PF13949 | 0.354 |
LIG_LYPXL_yS_3 | 188 | 191 | PF13949 | 0.554 |
LIG_MLH1_MIPbox_1 | 68 | 72 | PF16413 | 0.460 |
LIG_NRBOX | 173 | 179 | PF00104 | 0.485 |
LIG_NRP_CendR_1 | 540 | 543 | PF00754 | 0.634 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.471 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.471 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.471 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.468 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.505 |
LIG_SUMO_SIM_anti_2 | 382 | 388 | PF11976 | 0.435 |
LIG_TRAF2_1 | 509 | 512 | PF00917 | 0.578 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.471 |
LIG_TYR_ITSM | 184 | 191 | PF00017 | 0.420 |
LIG_UBA3_1 | 532 | 540 | PF00899 | 0.434 |
LIG_WRC_WIRS_1 | 184 | 189 | PF05994 | 0.505 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.604 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.693 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.593 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.470 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.725 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.679 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.460 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.460 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.476 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.602 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.741 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.695 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.582 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.711 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.563 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.731 |
MOD_GlcNHglycan | 472 | 476 | PF01048 | 0.745 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.648 |
MOD_GlcNHglycan | 512 | 516 | PF01048 | 0.411 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.529 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.540 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.614 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.760 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.403 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.689 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.271 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.460 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.449 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.796 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.507 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.544 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.441 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.554 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.589 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.525 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.471 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.588 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.463 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.449 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.496 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.602 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.501 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.548 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.461 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.726 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.646 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.478 |
MOD_SUMO_for_1 | 34 | 37 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 215 | 224 | PF00179 | 0.446 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 500 | 503 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 360 | 375 | PF08389 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR6 | Leptomonas seymouri | 65% | 100% |
A0A0S4KEA9 | Bodo saltans | 39% | 100% |
A0A1X0NT88 | Trypanosomatidae | 43% | 100% |
A0A422NXL8 | Trypanosoma rangeli | 45% | 100% |
A4H8Y5 | Leishmania braziliensis | 79% | 99% |
A4HXB5 | Leishmania infantum | 99% | 100% |
C9ZU02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AR11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QEF2 | Leishmania major | 92% | 100% |
V5BAJ7 | Trypanosoma cruzi | 42% | 87% |