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: A4HG31
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 | 0.551 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.346 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.346 |
CLV_PCSK_PC7_1 | 295 | 301 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.360 |
CLV_Separin_Metazoa | 477 | 481 | PF03568 | 0.565 |
DEG_APCC_DBOX_1 | 287 | 295 | PF00400 | 0.573 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.326 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.385 |
DEG_SCF_FBW7_1 | 196 | 203 | PF00400 | 0.585 |
DOC_CDC14_PxL_1 | 220 | 228 | PF14671 | 0.397 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.516 |
DOC_CYCLIN_RxL_1 | 591 | 600 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 363 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 487 | 495 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 509 | 518 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 189 | 196 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 426 | 434 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 594 | 601 | PF00069 | 0.484 |
DOC_PP1_RVXF_1 | 153 | 159 | PF00149 | 0.474 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 288 | 294 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 49 | 57 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 5 | 13 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.440 |
LIG_Actin_WH2_2 | 44 | 62 | PF00022 | 0.533 |
LIG_AP2alpha_1 | 468 | 472 | PF02296 | 0.527 |
LIG_BRCT_BRCA1_1 | 379 | 383 | PF00533 | 0.758 |
LIG_Clathr_ClatBox_1 | 596 | 600 | PF01394 | 0.473 |
LIG_EH1_1 | 208 | 216 | PF00400 | 0.453 |
LIG_eIF4E_1 | 148 | 154 | PF01652 | 0.512 |
LIG_eIF4E_1 | 209 | 215 | PF01652 | 0.285 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.442 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.474 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.503 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.661 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.640 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.426 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.731 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.536 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.685 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.610 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.442 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.672 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.460 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.514 |
LIG_GBD_Chelix_1 | 289 | 297 | PF00786 | 0.496 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 208 | 215 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 380 | 391 | PF02991 | 0.743 |
LIG_LIR_Gen_1 | 517 | 526 | PF02991 | 0.509 |
LIG_LIR_LC3C_4 | 127 | 131 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 517 | 523 | PF02991 | 0.508 |
LIG_NRBOX | 591 | 597 | PF00104 | 0.482 |
LIG_PCNA_PIPBox_1 | 265 | 274 | PF02747 | 0.289 |
LIG_PCNA_yPIPBox_3 | 258 | 272 | PF02747 | 0.288 |
LIG_PCNA_yPIPBox_3 | 580 | 593 | PF02747 | 0.538 |
LIG_PDZ_Class_3 | 597 | 602 | PF00595 | 0.491 |
LIG_Pex14_2 | 468 | 472 | PF04695 | 0.527 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.533 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.290 |
LIG_SH2_CRK | 427 | 431 | PF00017 | 0.487 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.490 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.474 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.420 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.528 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.506 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.640 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.528 |
LIG_Sin3_3 | 158 | 165 | PF02671 | 0.506 |
LIG_SUMO_SIM_par_1 | 594 | 600 | PF11976 | 0.356 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.589 |
LIG_TYR_ITIM | 207 | 212 | PF00017 | 0.526 |
LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.610 |
LIG_WW_3 | 186 | 190 | PF00397 | 0.540 |
MOD_CDK_SPxxK_3 | 232 | 239 | PF00069 | 0.519 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.681 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.467 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.427 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.534 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.615 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.584 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.512 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.486 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.432 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.656 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.574 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.665 |
MOD_GlcNHglycan | 486 | 490 | PF01048 | 0.594 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.495 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.599 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.606 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.545 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.599 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.508 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.588 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.364 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.556 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.471 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.663 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.713 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.554 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.537 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.460 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.468 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.626 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.487 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.650 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.516 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.528 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.376 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.497 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.249 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.320 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.544 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.581 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.417 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.318 |
MOD_PIKK_1 | 575 | 581 | PF00454 | 0.467 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.553 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.497 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.553 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.538 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.639 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.664 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.517 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.322 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.512 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.606 |
MOD_Plk_2-3 | 445 | 451 | PF00069 | 0.512 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.535 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.560 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.395 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.385 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.432 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.559 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.615 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.709 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.679 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 433 | 438 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 327 | 329 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.350 |
TRG_NES_CRM1_1 | 462 | 477 | PF08389 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 570 | 574 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS15 | Leptomonas seymouri | 65% | 100% |
A0A1X0NK92 | Trypanosomatidae | 31% | 100% |
A0A3R7KAG0 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X119 | Leishmania donovani | 84% | 100% |
C9ZJ53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ACX1 | Leishmania major | 84% | 100% |
E9AZG1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
V5BEQ8 | Trypanosoma cruzi | 33% | 100% |