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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QIG2
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 3 |
GO:0009889 | regulation of biosynthetic process | 4 | 3 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0010468 | regulation of gene expression | 5 | 3 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 3 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 3 |
GO:0019222 | regulation of metabolic process | 3 | 3 |
GO:0031323 | regulation of cellular metabolic process | 4 | 3 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 3 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 2 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 3 |
GO:0050794 | regulation of cellular process | 3 | 3 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 3 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 3 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 3 |
GO:0065007 | biological regulation | 1 | 3 |
GO:0080090 | regulation of primary metabolic process | 4 | 3 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 3 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003712 | transcription coregulator activity | 2 | 2 |
GO:0003713 | transcription coactivator activity | 3 | 2 |
GO:0140110 | transcription regulator activity | 1 | 2 |
GO:0005488 | binding | 1 | 1 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 621 | 623 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.435 |
CLV_PCSK_FUR_1 | 126 | 130 | PF00082 | 0.720 |
CLV_PCSK_FUR_1 | 233 | 237 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.719 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 505 | 507 | PF00082 | 0.417 |
CLV_PCSK_PC7_1 | 393 | 399 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.444 |
CLV_Separin_Metazoa | 52 | 56 | PF03568 | 0.332 |
DEG_APCC_DBOX_1 | 621 | 629 | PF00400 | 0.407 |
DEG_APCC_KENBOX_2 | 302 | 306 | PF00400 | 0.730 |
DEG_COP1_1 | 327 | 337 | PF00400 | 0.690 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.645 |
DEG_SPOP_SBC_1 | 98 | 102 | PF00917 | 0.591 |
DOC_CYCLIN_yCln2_LP_2 | 598 | 604 | PF00134 | 0.355 |
DOC_MAPK_DCC_7 | 596 | 604 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 125 | 133 | PF00069 | 0.687 |
DOC_MAPK_gen_1 | 427 | 435 | PF00069 | 0.606 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.592 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.578 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.289 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.378 |
DOC_SPAK_OSR1_1 | 474 | 478 | PF12202 | 0.469 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.575 |
DOC_USP7_UBL2_3 | 427 | 431 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.385 |
LIG_14-3-3_CanoR_1 | 137 | 146 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 482 | 490 | PF00244 | 0.488 |
LIG_APCC_ABBA_1 | 415 | 420 | PF00400 | 0.614 |
LIG_APCC_ABBAyCdc20_2 | 128 | 134 | PF00400 | 0.503 |
LIG_BH_BH3_1 | 18 | 34 | PF00452 | 0.442 |
LIG_BIR_III_4 | 13 | 17 | PF00653 | 0.481 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.482 |
LIG_Clathr_ClatBox_1 | 610 | 614 | PF01394 | 0.367 |
LIG_EH1_1 | 474 | 482 | PF00400 | 0.467 |
LIG_eIF4E_1 | 20 | 26 | PF01652 | 0.454 |
LIG_eIF4E_1 | 553 | 559 | PF01652 | 0.274 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.714 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.539 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.541 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.494 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.627 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.286 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.328 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.405 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.547 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.633 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.653 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.592 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.492 |
LIG_LIR_Apic_2 | 252 | 257 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 536 | 545 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 585 | 595 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.357 |
LIG_MAD2 | 331 | 339 | PF02301 | 0.589 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.274 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 20 | 24 | PF00017 | 0.474 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.274 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.274 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.629 |
LIG_SUMO_SIM_anti_2 | 430 | 436 | PF11976 | 0.695 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.432 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.588 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.576 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.742 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.573 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.274 |
MOD_CDC14_SPxK_1 | 471 | 474 | PF00782 | 0.416 |
MOD_CDK_SPxK_1 | 468 | 474 | PF00069 | 0.439 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.475 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.683 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.632 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.728 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.754 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.568 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.396 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.608 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.615 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.557 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.470 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.503 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.661 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.587 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.586 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.686 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.412 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.786 |
MOD_Cter_Amidation | 361 | 364 | PF01082 | 0.761 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.456 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.607 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.480 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.643 |
MOD_GlcNHglycan | 241 | 246 | PF01048 | 0.599 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.587 |
MOD_GlcNHglycan | 264 | 268 | PF01048 | 0.605 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.733 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.684 |
MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.676 |
MOD_GlcNHglycan | 465 | 469 | PF01048 | 0.677 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.464 |
MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.570 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.713 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.601 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.497 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.528 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.577 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.743 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.507 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.378 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.494 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.595 |
MOD_LATS_1 | 10 | 16 | PF00433 | 0.496 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.666 |
MOD_N-GLC_2 | 36 | 38 | PF02516 | 0.570 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.641 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.505 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.510 |
MOD_NEK2_2 | 155 | 160 | PF00069 | 0.504 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.610 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.782 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.346 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.697 |
MOD_PKA_1 | 137 | 143 | PF00069 | 0.613 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.637 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.697 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.680 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.539 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.637 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.768 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.497 |
MOD_PKB_1 | 81 | 89 | PF00069 | 0.497 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.591 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.661 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.663 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.581 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.552 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.598 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.173 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.482 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.399 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.543 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.535 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.500 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.708 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.626 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.665 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.462 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.352 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.377 |
MOD_SUMO_for_1 | 577 | 580 | PF00179 | 0.302 |
MOD_SUMO_rev_2 | 196 | 205 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 589 | 598 | PF00179 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.361 |
TRG_ER_FFAT_2 | 214 | 221 | PF00635 | 0.454 |
TRG_NLS_MonoExtC_3 | 124 | 129 | PF00514 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 623 | 627 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGL1 | Leptomonas seymouri | 67% | 100% |
A0A0S4IUQ4 | Bodo saltans | 38% | 98% |
A0A1X0NNW7 | Trypanosomatidae | 44% | 98% |
A0A3S5H626 | Leishmania donovani | 93% | 100% |
A0A3S5IQP6 | Trypanosoma rangeli | 48% | 100% |
A4H574 | Leishmania braziliensis | 77% | 100% |
A4HTF7 | Leishmania infantum | 93% | 100% |
C9ZPN3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AM85 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BH64 | Trypanosoma cruzi | 47% | 100% |