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: E9AWN0
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 | 553 | 557 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.442 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 617 | 619 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.455 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 592 | 596 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 654 | 658 | PF00082 | 0.432 |
CLV_Separin_Metazoa | 359 | 363 | PF03568 | 0.493 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.547 |
DEG_SCF_FBW7_1 | 599 | 606 | PF00400 | 0.467 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.446 |
DEG_SPOP_SBC_1 | 551 | 555 | PF00917 | 0.442 |
DOC_CKS1_1 | 600 | 605 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 123 | 135 | PF00134 | 0.468 |
DOC_CYCLIN_RxL_1 | 355 | 363 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 573 | 579 | PF00134 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 607 | 613 | PF00134 | 0.285 |
DOC_MAPK_gen_1 | 164 | 172 | PF00069 | 0.235 |
DOC_MAPK_gen_1 | 63 | 69 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 188 | 195 | PF00149 | 0.475 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.389 |
DOC_PP2B_LxvP_1 | 573 | 576 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.256 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 462 | 466 | PF12436 | 0.251 |
DOC_USP7_UBL2_3 | 654 | 658 | PF12436 | 0.433 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 493 | 501 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 502 | 508 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 639 | 643 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.360 |
LIG_APCC_ABBA_1 | 467 | 472 | PF00400 | 0.362 |
LIG_APCC_ABBAyCdc20_2 | 190 | 196 | PF00400 | 0.465 |
LIG_APCC_ABBAyCdc20_2 | 430 | 436 | PF00400 | 0.262 |
LIG_APCC_ABBAyCdc20_2 | 466 | 472 | PF00400 | 0.472 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_1 | 362 | 366 | PF00533 | 0.365 |
LIG_CSL_BTD_1 | 424 | 427 | PF09270 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 472 | 480 | PF00928 | 0.444 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.509 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.429 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.451 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.495 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.331 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.462 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.466 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.638 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.495 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.385 |
LIG_HCF-1_HBM_1 | 196 | 199 | PF13415 | 0.492 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.470 |
LIG_LIR_Apic_2 | 522 | 526 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 196 | 204 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 236 | 246 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 74 | 85 | PF02991 | 0.454 |
LIG_LIR_LC3C_4 | 504 | 508 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 271 | 276 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.443 |
LIG_MLH1_MIPbox_1 | 297 | 301 | PF16413 | 0.379 |
LIG_NRBOX | 569 | 575 | PF00104 | 0.451 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.496 |
LIG_Pex14_1 | 631 | 635 | PF04695 | 0.374 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.381 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.425 |
LIG_Pex14_2 | 83 | 87 | PF04695 | 0.455 |
LIG_PTB_Apo_2 | 338 | 345 | PF02174 | 0.360 |
LIG_PTB_Phospho_1 | 338 | 344 | PF10480 | 0.362 |
LIG_REV1ctd_RIR_1 | 298 | 306 | PF16727 | 0.322 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.528 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 70 | 73 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.445 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.531 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.340 |
LIG_SUMO_SIM_anti_2 | 169 | 174 | PF11976 | 0.488 |
LIG_SUMO_SIM_anti_2 | 566 | 572 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 327 | 332 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 566 | 572 | PF11976 | 0.453 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.521 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.582 |
LIG_WRC_WIRS_1 | 438 | 443 | PF05994 | 0.419 |
LIG_WRPW_2 | 101 | 104 | PF00400 | 0.491 |
MOD_CDK_SPxxK_3 | 423 | 430 | PF00069 | 0.390 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.603 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.407 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.423 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.690 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.546 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.237 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.265 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.485 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.476 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.664 |
MOD_CMANNOS | 101 | 104 | PF00535 | 0.491 |
MOD_CMANNOS | 364 | 367 | PF00535 | 0.360 |
MOD_Cter_Amidation | 354 | 357 | PF01082 | 0.319 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.498 |
MOD_GlcNHglycan | 205 | 209 | PF01048 | 0.599 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.394 |
MOD_GlcNHglycan | 387 | 391 | PF01048 | 0.478 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.460 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.522 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.451 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.749 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.543 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.580 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.482 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.444 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.343 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.500 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.709 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.542 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.504 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.501 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.341 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.343 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.468 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.522 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.419 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.279 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.417 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.460 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.461 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.429 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.433 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.490 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.406 |
MOD_NEK2_2 | 307 | 312 | PF00069 | 0.423 |
MOD_OFUCOSY | 304 | 311 | PF10250 | 0.329 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.573 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.481 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.481 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.526 |
MOD_PK_1 | 318 | 324 | PF00069 | 0.518 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.542 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.477 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.546 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.443 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.512 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.514 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.560 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.406 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.458 |
MOD_Plk_2-3 | 582 | 588 | PF00069 | 0.477 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.509 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.462 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.456 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.497 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.419 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.457 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.477 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 191 | 200 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 504 | 514 | PF00179 | 0.482 |
TRG_DiLeu_BaEn_1 | 428 | 433 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_3 | 323 | 329 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_4 | 60 | 66 | PF01217 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 127 | 132 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 405 | 410 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 616 | 618 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.455 |
TRG_NES_CRM1_1 | 452 | 465 | PF08389 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 164 | 169 | PF00026 | 0.252 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9W0 | Leptomonas seymouri | 65% | 100% |
A0A0S4J867 | Bodo saltans | 32% | 100% |
A0A1X0NIX9 | Trypanosomatidae | 38% | 98% |
A0A3S5H7C8 | Leishmania donovani | 92% | 100% |
A0A422P403 | Trypanosoma rangeli | 38% | 100% |
A4HD96 | Leishmania braziliensis | 85% | 100% |
D0A710 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AH51 | Leishmania infantum | 92% | 100% |
Q4QAU1 | Leishmania major | 90% | 100% |
V5BRA0 | Trypanosoma cruzi | 40% | 99% |