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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000428 | DNA-directed RNA polymerase complex | 4 | 10 |
GO:0005666 | RNA polymerase III complex | 4 | 10 |
GO:0030880 | RNA polymerase complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0055029 | nuclear DNA-directed RNA polymerase complex | 3 | 10 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 10 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
GO:0140535 | intracellular protein-containing complex | 2 | 10 |
GO:1902494 | catalytic complex | 2 | 10 |
GO:1990234 | transferase complex | 3 | 10 |
Related structures:
AlphaFold database: E9AZG1
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003697 | single-stranded DNA binding | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.656 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.654 |
CLV_PCSK_PC7_1 | 298 | 304 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 479 | 483 | PF03568 | 0.570 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.552 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.379 |
DEG_SCF_FBW7_1 | 196 | 203 | PF00400 | 0.577 |
DEG_SIAH_1 | 537 | 545 | PF03145 | 0.525 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.572 |
DOC_CYCLIN_RxL_1 | 593 | 602 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 360 | 366 | PF00134 | 0.540 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 511 | 520 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 189 | 196 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 428 | 436 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 596 | 603 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 153 | 159 | PF00149 | 0.471 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.706 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 482 | 490 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 44 | 62 | PF00022 | 0.511 |
LIG_AP2alpha_1 | 470 | 474 | PF02296 | 0.517 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.739 |
LIG_Clathr_ClatBox_1 | 598 | 602 | PF01394 | 0.470 |
LIG_EH1_1 | 208 | 216 | PF00400 | 0.446 |
LIG_eIF4E_1 | 148 | 154 | PF01652 | 0.491 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.437 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.517 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.603 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.410 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.570 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.540 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.609 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.616 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.435 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.665 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.242 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.508 |
LIG_GBD_Chelix_1 | 292 | 300 | PF00786 | 0.472 |
LIG_GBD_Chelix_1 | 43 | 51 | PF00786 | 0.368 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 208 | 215 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 316 | 325 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 382 | 393 | PF02991 | 0.691 |
LIG_LIR_Gen_1 | 458 | 466 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 519 | 528 | PF02991 | 0.516 |
LIG_LIR_LC3C_4 | 127 | 131 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 402 | 407 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 458 | 462 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.474 |
LIG_MAD2 | 298 | 306 | PF02301 | 0.295 |
LIG_NRBOX | 593 | 599 | PF00104 | 0.479 |
LIG_PCNA_yPIPBox_3 | 582 | 595 | PF02747 | 0.535 |
LIG_PDZ_Class_3 | 599 | 604 | PF00595 | 0.479 |
LIG_Pex14_2 | 470 | 474 | PF04695 | 0.517 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.526 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 459 | 462 | PF00017 | 0.461 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.629 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.504 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.471 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.523 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.654 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.381 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.525 |
LIG_SH3_4 | 397 | 404 | PF00018 | 0.538 |
LIG_Sin3_3 | 158 | 165 | PF02671 | 0.504 |
LIG_SUMO_SIM_par_1 | 596 | 602 | PF11976 | 0.368 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.559 |
LIG_TYR_ITIM | 207 | 212 | PF00017 | 0.519 |
LIG_WRC_WIRS_1 | 314 | 319 | PF05994 | 0.577 |
LIG_WW_3 | 186 | 190 | PF00397 | 0.532 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.611 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.475 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.685 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.527 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.518 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.585 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.236 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.471 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.441 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.602 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.614 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.534 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.231 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.561 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.579 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.413 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.604 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.619 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.542 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.677 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.481 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.478 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.699 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.485 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.711 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.658 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.686 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.463 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.386 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.234 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.455 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.225 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.320 |
MOD_NEK2_2 | 491 | 496 | PF00069 | 0.421 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.619 |
MOD_PK_1 | 198 | 204 | PF00069 | 0.534 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.477 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.643 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.645 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.552 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.507 |
MOD_Plk_2-3 | 447 | 453 | PF00069 | 0.507 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.486 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.554 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.414 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.389 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.428 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.551 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.578 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.450 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.713 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.692 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 593 | 598 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 300 | 303 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.636 |
TRG_NES_CRM1_1 | 464 | 479 | PF08389 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 449 | 453 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS15 | Leptomonas seymouri | 65% | 100% |
A0A1X0NK92 | Trypanosomatidae | 30% | 100% |
A0A3R7KAG0 | Trypanosoma rangeli | 31% | 100% |
A0A3S7X119 | Leishmania donovani | 95% | 100% |
A4HG31 | Leishmania braziliensis | 83% | 100% |
C9ZJ53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ACX1 | Leishmania major | 95% | 100% |
V5BEQ8 | Trypanosoma cruzi | 31% | 100% |