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:0000127 | transcription factor TFIIIC complex | 4 | 10 |
GO:0005667 | transcription regulator complex | 2 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0090576 | RNA polymerase III transcription regulator complex | 3 | 10 |
Related structures:
AlphaFold database: Q4QC86
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006352 | DNA-templated transcription initiation | 6 | 10 |
GO:0006384 | transcription initiation at RNA polymerase III promoter | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009059 | macromolecule biosynthetic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0018130 | heterocycle biosynthetic process | 4 | 10 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 10 |
GO:0032774 | RNA biosynthetic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.821 |
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.419 |
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.307 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.500 |
CLV_PCSK_FUR_1 | 214 | 218 | PF00082 | 0.698 |
CLV_PCSK_FUR_1 | 242 | 246 | PF00082 | 0.637 |
CLV_PCSK_FUR_1 | 540 | 544 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.651 |
CLV_PCSK_PC7_1 | 240 | 246 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 538 | 544 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 604 | 610 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.502 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.726 |
DEG_APCC_DBOX_1 | 554 | 562 | PF00400 | 0.478 |
DEG_SCF_FBW7_1 | 33 | 38 | PF00400 | 0.688 |
DEG_SCF_TRCP1_1 | 118 | 124 | PF00400 | 0.562 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.676 |
DEG_SPOP_SBC_1 | 660 | 664 | PF00917 | 0.696 |
DOC_CDC14_PxL_1 | 320 | 328 | PF14671 | 0.648 |
DOC_CKS1_1 | 314 | 319 | PF01111 | 0.640 |
DOC_CYCLIN_RxL_1 | 527 | 539 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 571 | 577 | PF00134 | 0.482 |
DOC_MAPK_gen_1 | 508 | 517 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 564 | 573 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 234 | 241 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 511 | 519 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 567 | 575 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 234 | 242 | PF00069 | 0.597 |
DOC_PP2B_LxvP_1 | 571 | 574 | PF13499 | 0.499 |
DOC_PP2B_PxIxI_1 | 390 | 396 | PF00149 | 0.425 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.545 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.653 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 504 | 508 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 555 | 559 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 609 | 617 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 498 | 513 | PF00022 | 0.425 |
LIG_BIR_III_4 | 280 | 284 | PF00653 | 0.615 |
LIG_BIR_III_4 | 375 | 379 | PF00653 | 0.362 |
LIG_BIR_III_4 | 648 | 652 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.721 |
LIG_BRCT_BRCA1_1 | 680 | 684 | PF00533 | 0.756 |
LIG_CtBP_PxDLS_1 | 599 | 603 | PF00389 | 0.562 |
LIG_eIF4E_1 | 232 | 238 | PF01652 | 0.519 |
LIG_EVH1_2 | 333 | 337 | PF00568 | 0.333 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.596 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.536 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.665 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.730 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.689 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.368 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.325 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.387 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.576 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.672 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.419 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.748 |
LIG_GBD_Chelix_1 | 446 | 454 | PF00786 | 0.419 |
LIG_Integrin_RGD_1 | 86 | 88 | PF01839 | 0.705 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 218 | 228 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 23 | 32 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 386 | 395 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 499 | 510 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.450 |
LIG_NRBOX | 531 | 537 | PF00104 | 0.481 |
LIG_NRBOX | 627 | 633 | PF00104 | 0.494 |
LIG_PCNA_PIPBox_1 | 226 | 235 | PF02747 | 0.525 |
LIG_PCNA_yPIPBox_3 | 226 | 240 | PF02747 | 0.516 |
LIG_PTB_Apo_2 | 227 | 234 | PF02174 | 0.631 |
LIG_PTB_Apo_2 | 476 | 483 | PF02174 | 0.333 |
LIG_PTB_Phospho_1 | 227 | 233 | PF10480 | 0.634 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.679 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 494 | 498 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 502 | 506 | PF00017 | 0.419 |
LIG_SH2_PTP2 | 24 | 27 | PF00017 | 0.652 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 617 | 621 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 624 | 628 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.438 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.590 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.435 |
LIG_SUMO_SIM_par_1 | 391 | 396 | PF11976 | 0.425 |
LIG_TRAF2_1 | 178 | 181 | PF00917 | 0.741 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.628 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.499 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.703 |
LIG_TRAF2_2 | 574 | 579 | PF00917 | 0.466 |
LIG_TYR_ITIM | 500 | 505 | PF00017 | 0.362 |
LIG_TYR_ITIM | 544 | 549 | PF00017 | 0.479 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.752 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.747 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.638 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.699 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.480 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.419 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.675 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.677 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.683 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.494 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.442 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.733 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.702 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.698 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.574 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.798 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.717 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.803 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.634 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.412 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.410 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.425 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.708 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.351 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.381 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.654 |
MOD_GlcNHglycan | 677 | 683 | PF01048 | 0.694 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.663 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.814 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.780 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.634 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.756 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.596 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.405 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.445 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.497 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.175 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.608 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.694 |
MOD_N-GLC_1 | 651 | 656 | PF02516 | 0.746 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.454 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.426 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.704 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.709 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.743 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.693 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.489 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.343 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.391 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.396 |
MOD_PKB_1 | 518 | 526 | PF00069 | 0.512 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.645 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.425 |
MOD_Plk_1 | 678 | 684 | PF00069 | 0.778 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.385 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.473 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.444 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.492 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.453 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.383 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.533 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.643 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.600 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.769 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.498 |
MOD_SUMO_rev_2 | 539 | 549 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 224 | 229 | PF01217 | 0.659 |
TRG_DiLeu_BaEn_2 | 60 | 66 | PF01217 | 0.690 |
TRG_DiLeu_BaEn_4 | 398 | 404 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 505 | 510 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 530 | 535 | PF01217 | 0.489 |
TRG_DiLeu_LyEn_5 | 635 | 640 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 546 | 549 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 239 | 242 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 542 | 544 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.536 |
TRG_NLS_MonoCore_2 | 212 | 217 | PF00514 | 0.695 |
TRG_NLS_MonoExtC_3 | 212 | 217 | PF00514 | 0.695 |
TRG_NLS_MonoExtN_4 | 210 | 217 | PF00514 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 641 | 646 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I9 | Leptomonas seymouri | 50% | 94% |
A0A1X0NZE8 | Trypanosomatidae | 32% | 100% |
A0A3S7WWK4 | Leishmania donovani | 93% | 100% |
A0A422NAG1 | Trypanosoma rangeli | 34% | 100% |
A4HIW4 | Leishmania braziliensis | 80% | 100% |
D0A185 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGX8 | Leishmania infantum | 92% | 100% |
E9AV94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |