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: Q4QEF2
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 | 0.520 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.342 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.481 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.465 |
DOC_CYCLIN_RxL_1 | 147 | 158 | PF00134 | 0.549 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.479 |
DOC_MAPK_FxFP_2 | 533 | 536 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 371 | 379 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 434 | 443 | PF00069 | 0.537 |
DOC_MAPK_RevD_3 | 63 | 78 | PF00069 | 0.550 |
DOC_PIKK_1 | 169 | 177 | PF02985 | 0.550 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.465 |
DOC_PP1_RVXF_1 | 33 | 39 | PF00149 | 0.288 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.465 |
DOC_PP4_FxxP_1 | 533 | 536 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.488 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 234 | 242 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 26 | 30 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 220 | 236 | PF00022 | 0.477 |
LIG_APCC_ABBA_1 | 302 | 307 | PF00400 | 0.642 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.454 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.457 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.473 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.456 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.712 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.482 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.495 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.465 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.475 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.785 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.556 |
LIG_LIR_Apic_2 | 115 | 119 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 495 | 500 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 530 | 536 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.454 |
LIG_LYPXL_S_1 | 187 | 191 | PF13949 | 0.350 |
LIG_LYPXL_yS_3 | 188 | 191 | PF13949 | 0.550 |
LIG_MLH1_MIPbox_1 | 68 | 72 | PF16413 | 0.454 |
LIG_NRBOX | 173 | 179 | PF00104 | 0.479 |
LIG_NRP_CendR_1 | 552 | 555 | PF00754 | 0.613 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.465 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.465 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.465 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.462 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.497 |
LIG_TRAF2_1 | 521 | 524 | PF00917 | 0.572 |
LIG_TYR_ITIM | 194 | 199 | PF00017 | 0.465 |
LIG_UBA3_1 | 544 | 552 | PF00899 | 0.423 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.596 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.648 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.701 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.475 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.715 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.618 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.454 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.454 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.463 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.557 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.751 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.654 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.516 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.679 |
MOD_GlcNHglycan | 400 | 404 | PF01048 | 0.733 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.531 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.599 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.703 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.699 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.526 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.550 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.786 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.687 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.265 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.202 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.459 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.366 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.492 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.542 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.428 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.544 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.588 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.525 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.465 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.574 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.505 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.457 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.449 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.558 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.454 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.503 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.643 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.656 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.474 |
MOD_SUMO_for_1 | 34 | 37 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 215 | 224 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 514 | 520 | PF00179 | 0.359 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.509 |
TRG_NES_CRM1_1 | 360 | 375 | PF08389 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR6 | Leptomonas seymouri | 64% | 100% |
A0A0S4KEA9 | Bodo saltans | 38% | 100% |
A0A1X0NT88 | Trypanosomatidae | 41% | 100% |
A0A3Q8IDX6 | Leishmania donovani | 92% | 100% |
A0A422NXL8 | Trypanosoma rangeli | 43% | 100% |
A4H8Y5 | Leishmania braziliensis | 81% | 100% |
A4HXB5 | Leishmania infantum | 92% | 100% |
C9ZU02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AR11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BAJ7 | Trypanosoma cruzi | 42% | 89% |