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: 20 |
NetGPI | no | yes: 0, no: 20 |
Related structures:
AlphaFold database: A4I1M6
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 3 |
GO:0032259 | methylation | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 20 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008716 | D-alanine-D-alanine ligase activity | 5 | 17 |
GO:0016740 | transferase activity | 2 | 17 |
GO:0016874 | ligase activity | 2 | 17 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 17 |
GO:0016881 | acid-amino acid ligase activity | 4 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0043169 | cation binding | 3 | 17 |
GO:0046872 | metal ion binding | 4 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.341 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.487 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.224 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.486 |
CLV_PCSK_PC7_1 | 470 | 476 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.502 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.399 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.450 |
DEG_SPOP_SBC_1 | 494 | 498 | PF00917 | 0.455 |
DEG_SPOP_SBC_1 | 511 | 515 | PF00917 | 0.740 |
DOC_CYCLIN_RxL_1 | 326 | 337 | PF00134 | 0.318 |
DOC_CYCLIN_RxL_1 | 446 | 454 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.424 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 44 | 53 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 76 | 83 | PF00069 | 0.277 |
DOC_MAPK_NFAT4_5 | 76 | 84 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 105 | 112 | PF00149 | 0.418 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 240 | 246 | PF00149 | 0.422 |
DOC_PP1_RVXF_1 | 387 | 394 | PF00149 | 0.357 |
DOC_PP1_RVXF_1 | 428 | 435 | PF00149 | 0.349 |
DOC_PP4_FxxP_1 | 434 | 437 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.479 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.585 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.366 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.380 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 25 | 35 | PF00244 | 0.217 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 376 | 383 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.399 |
LIG_BRCT_BRCA1_1 | 430 | 434 | PF00533 | 0.340 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 283 | 291 | PF00928 | 0.301 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.430 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.304 |
LIG_Integrin_RGD_1 | 365 | 367 | PF01839 | 0.403 |
LIG_LIR_Apic_2 | 431 | 437 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 119 | 126 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 192 | 198 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 253 | 261 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 274 | 280 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 192 | 197 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.418 |
LIG_NRP_CendR_1 | 528 | 529 | PF00754 | 0.492 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.450 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.446 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.398 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.430 |
LIG_SH2_CRK | 220 | 224 | PF00017 | 0.430 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.333 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.411 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.440 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.441 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.375 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.366 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.419 |
LIG_TYR_ITAM | 207 | 223 | PF00017 | 0.430 |
LIG_TYR_ITIM | 238 | 243 | PF00017 | 0.458 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.464 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.515 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.400 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.564 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.524 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.621 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.503 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.508 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.479 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.357 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.244 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.333 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.536 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.545 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.527 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.550 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.545 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.459 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.546 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.287 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.441 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.436 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.333 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.577 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.476 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.589 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.473 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.516 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.405 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.416 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.504 |
MOD_N-GLC_2 | 38 | 40 | PF02516 | 0.391 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.402 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.410 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.513 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.506 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.407 |
MOD_PKA_1 | 473 | 479 | PF00069 | 0.472 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.288 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.407 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.481 |
MOD_PKB_1 | 159 | 167 | PF00069 | 0.407 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.458 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.489 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.470 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.476 |
MOD_Plk_2-3 | 403 | 409 | PF00069 | 0.460 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.435 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.508 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.430 |
MOD_SUMO_rev_2 | 192 | 202 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.343 |
MOD_SUMO_rev_2 | 73 | 82 | PF00179 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.627 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 158 | 161 | PF00400 | 0.407 |
TRG_NLS_Bipartite_1 | 455 | 477 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 470 | 477 | PF00514 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 450 | 454 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILV0 | Leptomonas seymouri | 38% | 100% |
A0A0S4JLQ2 | Bodo saltans | 38% | 100% |
A0A0S4JPH7 | Bodo saltans | 61% | 82% |
A0A1X0P879 | Trypanosomatidae | 37% | 100% |
A0A1X0P8J8 | Trypanosomatidae | 23% | 100% |
A0A3Q8ID63 | Leishmania donovani | 37% | 100% |
A0A3R7MWC4 | Trypanosoma rangeli | 38% | 100% |
A0A3R7P2U3 | Trypanosoma rangeli | 24% | 100% |
A0A422NGJ1 | Trypanosoma rangeli | 75% | 68% |
A4HFA0 | Leishmania braziliensis | 38% | 100% |
A4HNM9 | Leishmania braziliensis | 21% | 100% |
A4I2H5 | Leishmania infantum | 37% | 100% |
C9ZK70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 69% |
C9ZX10 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AYN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4Q8T5 | Leishmania major | 38% | 100% |
V5B7P8 | Trypanosoma cruzi | 37% | 100% |
V5BHW2 | Trypanosoma cruzi | 70% | 100% |
V5BQK1 | Trypanosoma cruzi | 23% | 100% |