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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QAU1
Term | Name | Level | Count |
---|---|---|---|
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0040029 | epigenetic regulation of gene expression | 6 | 2 |
GO:0045814 | negative regulation of gene expression, epigenetic | 7 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008276 | protein methyltransferase activity | 3 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 2 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 2 |
GO:0042054 | histone methyltransferase activity | 4 | 2 |
GO:0042799 | histone H4K20 methyltransferase activity | 6 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0005102 | signaling receptor binding | 3 | 3 |
GO:0005179 | hormone activity | 5 | 3 |
GO:0005184 | neuropeptide hormone activity | 6 | 3 |
GO:0005488 | binding | 1 | 4 |
GO:0005515 | protein binding | 2 | 4 |
GO:0030545 | signaling receptor regulator activity | 2 | 3 |
GO:0030546 | signaling receptor activator activity | 3 | 3 |
GO:0048018 | receptor ligand activity | 4 | 3 |
GO:0098772 | molecular function regulator activity | 1 | 3 |
GO:0140677 | molecular function activator activity | 2 | 3 |
GO:0030544 | Hsp70 protein binding | 4 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
GO:0051879 | Hsp90 protein binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 554 | 558 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 586 | 590 | PF00656 | 0.374 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.405 |
CLV_Separin_Metazoa | 360 | 364 | PF03568 | 0.483 |
CLV_Separin_Metazoa | 437 | 441 | PF03568 | 0.279 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.527 |
DEG_SPOP_SBC_1 | 552 | 556 | PF00917 | 0.378 |
DOC_CYCLIN_RxL_1 | 124 | 136 | PF00134 | 0.384 |
DOC_CYCLIN_RxL_1 | 356 | 364 | PF00134 | 0.414 |
DOC_CYCLIN_yCln2_LP_2 | 574 | 580 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 599 | 605 | PF00134 | 0.354 |
DOC_MAPK_gen_1 | 64 | 70 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 189 | 196 | PF00149 | 0.402 |
DOC_PP1_RVXF_1 | 200 | 206 | PF00149 | 0.357 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.420 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.313 |
DOC_USP7_UBL2_3 | 655 | 659 | PF12436 | 0.406 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 440 | 449 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 640 | 644 | PF00244 | 0.537 |
LIG_APCC_ABBA_1 | 468 | 473 | PF00400 | 0.339 |
LIG_APCC_ABBAyCdc20_2 | 191 | 197 | PF00400 | 0.513 |
LIG_APCC_ABBAyCdc20_2 | 467 | 473 | PF00400 | 0.458 |
LIG_BIR_III_4 | 20 | 24 | PF00653 | 0.289 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.347 |
LIG_CSL_BTD_1 | 425 | 428 | PF09270 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 473 | 481 | PF00928 | 0.427 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.530 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.421 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.436 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.477 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.323 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.396 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.451 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.596 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.441 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.431 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.461 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.593 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.364 |
LIG_HCF-1_HBM_1 | 197 | 200 | PF13415 | 0.479 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.450 |
LIG_LIR_Apic_2 | 523 | 527 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 272 | 277 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.423 |
LIG_MLH1_MIPbox_1 | 298 | 302 | PF16413 | 0.357 |
LIG_NRBOX | 570 | 576 | PF00104 | 0.431 |
LIG_NRBOX | 65 | 71 | PF00104 | 0.476 |
LIG_PCNA_PIPBox_1 | 218 | 227 | PF02747 | 0.267 |
LIG_Pex14_1 | 632 | 636 | PF04695 | 0.340 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.346 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.332 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.447 |
LIG_PTB_Apo_2 | 339 | 346 | PF02174 | 0.332 |
LIG_PTB_Phospho_1 | 339 | 345 | PF10480 | 0.333 |
LIG_REV1ctd_RIR_1 | 299 | 307 | PF16727 | 0.299 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.459 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.317 |
LIG_SH2_GRB2like | 71 | 74 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 200 | 204 | PF00017 | 0.459 |
LIG_SH2_NCK_1 | 320 | 324 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.423 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.517 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.311 |
LIG_SUMO_SIM_anti_2 | 170 | 175 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 567 | 573 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 328 | 333 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 544 | 550 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 567 | 573 | PF11976 | 0.436 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.358 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.454 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.495 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.392 |
LIG_WRPW_2 | 102 | 105 | PF00400 | 0.474 |
MOD_CDK_SPxxK_3 | 424 | 431 | PF00069 | 0.341 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.548 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.405 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.453 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.629 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.527 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.181 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.514 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.410 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.462 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.447 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.460 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.611 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.362 |
MOD_CMANNOS | 102 | 105 | PF00535 | 0.474 |
MOD_CMANNOS | 365 | 368 | PF00535 | 0.339 |
MOD_Cter_Amidation | 236 | 239 | PF01082 | 0.307 |
MOD_Cter_Amidation | 355 | 358 | PF01082 | 0.295 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.487 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.575 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.365 |
MOD_GlcNHglycan | 388 | 392 | PF01048 | 0.494 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.419 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.501 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.689 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.513 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.524 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.544 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.406 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.456 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.493 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.571 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.517 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.506 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.424 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.304 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.313 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.418 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.481 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.411 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.402 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.391 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.436 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.442 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.393 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.674 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.414 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.459 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.384 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.398 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.263 |
MOD_OFUCOSY | 305 | 312 | PF10250 | 0.302 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.526 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.462 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.465 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.492 |
MOD_PK_1 | 319 | 325 | PF00069 | 0.479 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.526 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.456 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.395 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.515 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.419 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.513 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.538 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.463 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.401 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.404 |
MOD_Plk_2-3 | 583 | 589 | PF00069 | 0.454 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.424 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.437 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.493 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.384 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.432 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 192 | 201 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 505 | 515 | PF00179 | 0.405 |
TRG_DiLeu_BaEn_3 | 324 | 330 | PF01217 | 0.407 |
TRG_DiLeu_BaEn_4 | 61 | 67 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.316 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 612 | 617 | PF01217 | 0.316 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.395 |
TRG_ER_FFAT_2 | 444 | 453 | PF00635 | 0.361 |
TRG_NES_CRM1_1 | 453 | 466 | PF08389 | 0.358 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9W0 | Leptomonas seymouri | 66% | 100% |
A0A0S4J867 | Bodo saltans | 31% | 100% |
A0A1X0NIX9 | Trypanosomatidae | 38% | 98% |
A0A3S5H7C8 | Leishmania donovani | 94% | 100% |
A0A422P403 | Trypanosoma rangeli | 38% | 100% |
A4HD96 | Leishmania braziliensis | 84% | 100% |
D0A710 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AH51 | Leishmania infantum | 93% | 100% |
E9AWN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BRA0 | Trypanosoma cruzi | 39% | 99% |