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: E9AH51
Term | Name | Level | Count |
---|---|---|---|
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0040029 | epigenetic regulation of gene expression | 6 | 1 |
GO:0045814 | negative regulation of gene expression, epigenetic | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0042799 | histone H4K20 methyltransferase activity | 6 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
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 | 555 | 559 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.439 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 358 | 360 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.439 |
CLV_Separin_Metazoa | 361 | 365 | PF03568 | 0.493 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.554 |
DEG_SCF_FBW7_1 | 601 | 608 | PF00400 | 0.479 |
DEG_SPOP_SBC_1 | 553 | 557 | PF00917 | 0.425 |
DOC_CKS1_1 | 449 | 454 | PF01111 | 0.329 |
DOC_CKS1_1 | 602 | 607 | PF01111 | 0.490 |
DOC_CYCLIN_RxL_1 | 125 | 137 | PF00134 | 0.464 |
DOC_CYCLIN_RxL_1 | 357 | 365 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 575 | 581 | PF00134 | 0.352 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 167 | 174 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 190 | 197 | PF00149 | 0.469 |
DOC_PP1_RVXF_1 | 201 | 207 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 575 | 578 | PF13499 | 0.459 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 656 | 660 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 141 | 149 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 495 | 503 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 641 | 645 | PF00244 | 0.549 |
LIG_APCC_ABBA_1 | 469 | 474 | PF00400 | 0.365 |
LIG_APCC_ABBAyCdc20_2 | 192 | 198 | PF00400 | 0.459 |
LIG_APCC_ABBAyCdc20_2 | 468 | 474 | PF00400 | 0.476 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.364 |
LIG_CSL_BTD_1 | 426 | 429 | PF09270 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 474 | 482 | PF00928 | 0.443 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.419 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.448 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.501 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.332 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.460 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.463 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.599 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.472 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.460 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.478 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.614 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.386 |
LIG_HCF-1_HBM_1 | 198 | 201 | PF13415 | 0.493 |
LIG_LIR_Apic_2 | 126 | 132 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 446 | 452 | PF02991 | 0.337 |
LIG_LIR_Apic_2 | 524 | 528 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 198 | 206 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.438 |
LIG_MLH1_MIPbox_1 | 299 | 303 | PF16413 | 0.374 |
LIG_MYND_1 | 607 | 611 | PF01753 | 0.314 |
LIG_NRBOX | 571 | 577 | PF00104 | 0.448 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.489 |
LIG_Pex14_1 | 633 | 637 | PF04695 | 0.366 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.370 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.420 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.461 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.356 |
LIG_PTB_Phospho_1 | 340 | 346 | PF10480 | 0.357 |
LIG_REV1ctd_RIR_1 | 300 | 308 | PF16727 | 0.318 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.515 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.341 |
LIG_SH2_GRB2like | 72 | 75 | PF00017 | 0.352 |
LIG_SH2_NCK_1 | 201 | 205 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 321 | 325 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.439 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.535 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.336 |
LIG_SUMO_SIM_anti_2 | 171 | 176 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 568 | 574 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 329 | 334 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 545 | 551 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 568 | 574 | PF11976 | 0.449 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.516 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.553 |
LIG_WRC_WIRS_1 | 440 | 445 | PF05994 | 0.426 |
LIG_WRPW_2 | 103 | 106 | PF00400 | 0.489 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.569 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.399 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.461 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.663 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.529 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.232 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.522 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.481 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.482 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.453 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.637 |
MOD_CMANNOS | 103 | 106 | PF00535 | 0.489 |
MOD_CMANNOS | 366 | 369 | PF00535 | 0.357 |
MOD_Cter_Amidation | 356 | 359 | PF01082 | 0.319 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.505 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.388 |
MOD_GlcNHglycan | 389 | 393 | PF01048 | 0.481 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.457 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.525 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.447 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.719 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.526 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.544 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.476 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.441 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.508 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.496 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.667 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.526 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.516 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.485 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.339 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.339 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.463 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.418 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.276 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.412 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.459 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.460 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.435 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.430 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.400 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.420 |
MOD_OFUCOSY | 306 | 313 | PF10250 | 0.325 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.536 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.472 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.491 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.514 |
MOD_PK_1 | 320 | 326 | PF00069 | 0.514 |
MOD_PKA_1 | 141 | 147 | PF00069 | 0.533 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.468 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.544 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.434 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.510 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.502 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.547 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.406 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.455 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.473 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.491 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.476 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.454 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.494 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.415 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.447 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.333 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 193 | 202 | PF00179 | 0.485 |
MOD_SUMO_rev_2 | 506 | 516 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_3 | 325 | 331 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_4 | 62 | 68 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 129 | 134 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 407 | 412 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 613 | 618 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 271 | 274 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.445 |
TRG_ER_FFAT_2 | 445 | 454 | PF00635 | 0.416 |
TRG_NES_CRM1_1 | 454 | 467 | PF08389 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9W0 | Leptomonas seymouri | 66% | 100% |
A0A0S4J867 | Bodo saltans | 31% | 100% |
A0A1X0NIX9 | Trypanosomatidae | 37% | 98% |
A0A3S5H7C8 | Leishmania donovani | 100% | 100% |
A0A422P403 | Trypanosoma rangeli | 39% | 100% |
A4HD96 | Leishmania braziliensis | 85% | 100% |
D0A710 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AWN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QAU1 | Leishmania major | 93% | 100% |
V5BRA0 | Trypanosoma cruzi | 39% | 100% |