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: A4H8Y5
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 | 351 | 355 | PF00656 | 0.508 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.328 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.363 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.486 |
DOC_AGCK_PIF_2 | 105 | 110 | PF00069 | 0.377 |
DOC_CKS1_1 | 59 | 64 | PF01111 | 0.452 |
DOC_CYCLIN_RxL_1 | 144 | 152 | PF00134 | 0.544 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.466 |
DOC_MAPK_FxFP_2 | 525 | 528 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 365 | 373 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 428 | 437 | PF00069 | 0.473 |
DOC_MAPK_RevD_3 | 57 | 72 | PF00069 | 0.542 |
DOC_PIKK_1 | 163 | 171 | PF02985 | 0.542 |
DOC_PP1_RVXF_1 | 153 | 159 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 27 | 33 | PF00149 | 0.262 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.452 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.434 |
DOC_USP7_UBL2_3 | 147 | 151 | PF12436 | 0.488 |
DOC_USP7_UBL2_3 | 381 | 385 | PF12436 | 0.661 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 214 | 230 | PF00022 | 0.463 |
LIG_APCC_ABBA_1 | 296 | 301 | PF00400 | 0.661 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 96 | 105 | PF00928 | 0.377 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.450 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.441 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.590 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.444 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.495 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.471 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.452 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.494 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.456 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.539 |
LIG_Integrin_RGD_1 | 72 | 74 | PF01839 | 0.327 |
LIG_LIR_Apic_2 | 109 | 113 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 522 | 528 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.465 |
LIG_LYPXL_S_1 | 181 | 185 | PF13949 | 0.342 |
LIG_LYPXL_yS_3 | 182 | 185 | PF13949 | 0.542 |
LIG_MLH1_MIPbox_1 | 62 | 66 | PF16413 | 0.441 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.466 |
LIG_NRP_CendR_1 | 544 | 547 | PF00754 | 0.557 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.452 |
LIG_Pex14_2 | 32 | 36 | PF04695 | 0.452 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.452 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 493 | 497 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.542 |
LIG_SH2_STAT3 | 95 | 98 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.477 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.484 |
LIG_Sin3_3 | 8 | 15 | PF02671 | 0.477 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.558 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.452 |
LIG_UBA3_1 | 529 | 534 | PF00899 | 0.377 |
LIG_UBA3_1 | 536 | 544 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 346 | 351 | PF05994 | 0.326 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.588 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.499 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.441 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.655 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.541 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.716 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.628 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.341 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.455 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.441 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.447 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.387 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.555 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.533 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.540 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.501 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.740 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.638 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.280 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.680 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.523 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.699 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.453 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.522 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.547 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.577 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.714 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.252 |
MOD_N-GLC_2 | 337 | 339 | PF02516 | 0.451 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.442 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.499 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.496 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.643 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.734 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.462 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.442 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.502 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.528 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.452 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.514 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.500 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.382 |
MOD_Plk_2-3 | 163 | 169 | PF00069 | 0.470 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.447 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.577 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.449 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.408 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.465 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 270 | 273 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 209 | 218 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_1 | 163 | 168 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.480 |
TRG_NES_CRM1_1 | 354 | 369 | PF08389 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR6 | Leptomonas seymouri | 62% | 100% |
A0A0S4KEA9 | Bodo saltans | 38% | 100% |
A0A1X0NT88 | Trypanosomatidae | 42% | 100% |
A0A3Q8IDX6 | Leishmania donovani | 79% | 100% |
A0A422NXL8 | Trypanosoma rangeli | 42% | 100% |
A4HXB5 | Leishmania infantum | 79% | 100% |
C9ZU02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AR11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 98% |
Q4QEF2 | Leishmania major | 81% | 100% |
V5BAJ7 | Trypanosoma cruzi | 42% | 87% |