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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A0A3Q8ICH7
Term | Name | Level | Count |
---|---|---|---|
GO:0001932 | regulation of protein phosphorylation | 7 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901407 | obsolete regulation of phosphorylation of RNA polymerase II C-terminal domain | 8 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016853 | isomerase activity | 2 | 7 |
GO:0016859 | cis-trans isomerase activity | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.454 |
CLV_PCSK_FUR_1 | 321 | 325 | PF00082 | 0.630 |
CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 218 | 220 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 678 | 680 | PF00082 | 0.656 |
CLV_PCSK_PC7_1 | 215 | 221 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 674 | 680 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.549 |
CLV_Separin_Metazoa | 42 | 46 | PF03568 | 0.467 |
CLV_Separin_Metazoa | 437 | 441 | PF03568 | 0.412 |
DEG_APCC_DBOX_1 | 680 | 688 | PF00400 | 0.423 |
DOC_CYCLIN_RxL_1 | 131 | 138 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 215 | 225 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 674 | 684 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 304 | 311 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 473 | 482 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 559 | 568 | PF00069 | 0.520 |
DOC_MAPK_RevD_3 | 354 | 369 | PF00069 | 0.641 |
DOC_PP2B_PxIxI_1 | 477 | 483 | PF00149 | 0.582 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.576 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.550 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 142 | 151 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 24 | 31 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 289 | 295 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 353 | 359 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 406 | 413 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 548 | 553 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 611 | 619 | PF00244 | 0.470 |
LIG_Actin_WH2_2 | 304 | 322 | PF00022 | 0.608 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.503 |
LIG_BIR_III_2 | 172 | 176 | PF00653 | 0.626 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.483 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.620 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.575 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.570 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.518 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.548 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.562 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.540 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.810 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.471 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.548 |
LIG_Integrin_RGD_1 | 578 | 580 | PF01839 | 0.554 |
LIG_IRF3_LxIS_1 | 40 | 47 | PF10401 | 0.472 |
LIG_LIR_Apic_2 | 357 | 361 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 378 | 388 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 39 | 48 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 633 | 641 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 387 | 392 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 607 | 612 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 626 | 632 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 633 | 637 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 638 | 644 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.476 |
LIG_NRBOX | 136 | 142 | PF00104 | 0.513 |
LIG_NRP_CendR_1 | 698 | 700 | PF00754 | 0.500 |
LIG_PTB_Apo_2 | 504 | 511 | PF02174 | 0.555 |
LIG_PTB_Phospho_1 | 504 | 510 | PF10480 | 0.613 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.614 |
LIG_SH2_PTP2 | 306 | 309 | PF00017 | 0.564 |
LIG_SH2_PTP2 | 381 | 384 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 448 | 451 | PF00017 | 0.512 |
LIG_SH2_SRC | 243 | 246 | PF00017 | 0.685 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.584 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.572 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.732 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.451 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.689 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.505 |
LIG_SUMO_SIM_anti_2 | 434 | 442 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 501 | 506 | PF11976 | 0.579 |
LIG_SUMO_SIM_anti_2 | 562 | 568 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 178 | 186 | PF11976 | 0.598 |
LIG_SUMO_SIM_par_1 | 82 | 87 | PF11976 | 0.538 |
LIG_TYR_ITIM | 627 | 632 | PF00017 | 0.302 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.684 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.508 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.612 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.744 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.404 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.500 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.499 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.597 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.483 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.759 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.652 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.306 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.628 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.638 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.648 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.608 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.644 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.540 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.523 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.636 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.533 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.342 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.632 |
MOD_GlcNHglycan | 92 | 96 | PF01048 | 0.521 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.623 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.628 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.499 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.768 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.647 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.596 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.489 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.559 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.594 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.623 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.438 |
MOD_N-GLC_1 | 560 | 565 | PF02516 | 0.515 |
MOD_N-GLC_2 | 102 | 104 | PF02516 | 0.492 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.582 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.501 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.588 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.456 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.585 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.489 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.363 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.496 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.524 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.503 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.620 |
MOD_NEK2_2 | 458 | 463 | PF00069 | 0.568 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.363 |
MOD_PIKK_1 | 659 | 665 | PF00454 | 0.446 |
MOD_PKA_1 | 368 | 374 | PF00069 | 0.650 |
MOD_PKA_1 | 548 | 554 | PF00069 | 0.607 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.497 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.650 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.494 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.472 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.662 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.318 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.518 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.508 |
MOD_Plk_1 | 560 | 566 | PF00069 | 0.516 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.525 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.507 |
MOD_Plk_2-3 | 633 | 639 | PF00069 | 0.366 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.504 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.449 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.625 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.760 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.415 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.569 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.647 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.445 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.648 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.697 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.604 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.510 |
MOD_SUMO_rev_2 | 576 | 584 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 614 | 623 | PF00179 | 0.302 |
TRG_DiLeu_BaEn_1 | 434 | 439 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_1 | 562 | 567 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 475 | 480 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 676 | 679 | PF00400 | 0.493 |
TRG_NLS_Bipartite_1 | 207 | 222 | PF00514 | 0.521 |
TRG_NLS_MonoCore_2 | 217 | 222 | PF00514 | 0.570 |
TRG_NLS_MonoExtN_4 | 215 | 222 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 543 | 547 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 649 | 653 | PF00026 | 0.363 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB00 | Leptomonas seymouri | 57% | 100% |
A4H8I6 | Leishmania braziliensis | 81% | 100% |
A4HWW3 | Leishmania infantum | 99% | 100% |
E9AQM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QEV5 | Leishmania major | 87% | 100% |