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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AQM3
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 |
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018208 | peptidyl-proline modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016853 | isomerase activity | 2 | 8 |
GO:0016859 | cis-trans isomerase activity | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.721 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.705 |
CLV_PCSK_FUR_1 | 273 | 277 | PF00082 | 0.773 |
CLV_PCSK_FUR_1 | 318 | 322 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 633 | 635 | PF00082 | 0.641 |
CLV_PCSK_PC7_1 | 167 | 173 | PF00082 | 0.689 |
CLV_PCSK_PC7_1 | 358 | 364 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 629 | 635 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.644 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.758 |
DEG_SPOP_SBC_1 | 287 | 291 | PF00917 | 0.511 |
DOC_CYCLIN_RxL_1 | 83 | 90 | PF00134 | 0.704 |
DOC_MAPK_gen_1 | 167 | 177 | PF00069 | 0.680 |
DOC_MAPK_gen_1 | 629 | 639 | PF00069 | 0.715 |
DOC_MAPK_MEF2A_6 | 256 | 263 | PF00069 | 0.687 |
DOC_MAPK_MEF2A_6 | 428 | 437 | PF00069 | 0.765 |
DOC_MAPK_MEF2A_6 | 514 | 523 | PF00069 | 0.623 |
DOC_MAPK_RevD_3 | 306 | 321 | PF00069 | 0.771 |
DOC_PP2B_PxIxI_1 | 432 | 438 | PF00149 | 0.754 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 361 | 368 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 395 | 399 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 488 | 495 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 566 | 574 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 579 | 583 | PF00244 | 0.555 |
LIG_Actin_WH2_2 | 256 | 274 | PF00022 | 0.721 |
LIG_BIR_III_2 | 124 | 128 | PF00653 | 0.700 |
LIG_BIR_III_4 | 476 | 480 | PF00653 | 0.627 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.691 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.618 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.619 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.493 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.572 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.634 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.731 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.625 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.612 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.798 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.500 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.547 |
LIG_Integrin_RGD_1 | 533 | 535 | PF01839 | 0.678 |
LIG_LIR_Apic_2 | 309 | 313 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 330 | 340 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 49 | 60 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 588 | 596 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.761 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 562 | 567 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.554 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.617 |
LIG_PTB_Apo_2 | 459 | 466 | PF02174 | 0.641 |
LIG_PTB_Phospho_1 | 459 | 465 | PF10480 | 0.764 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.744 |
LIG_SH2_PTP2 | 258 | 261 | PF00017 | 0.639 |
LIG_SH2_PTP2 | 333 | 336 | PF00017 | 0.775 |
LIG_SH2_PTP2 | 403 | 406 | PF00017 | 0.621 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.735 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.738 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.800 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.775 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.716 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.661 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.685 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.775 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 456 | 461 | PF11976 | 0.653 |
LIG_SUMO_SIM_anti_2 | 517 | 523 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 34 | 39 | PF11976 | 0.615 |
LIG_TYR_ITIM | 582 | 587 | PF00017 | 0.376 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.775 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.601 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.622 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.690 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.468 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.450 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.585 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.661 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.376 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.517 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.663 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.698 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.758 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.688 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.492 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.683 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.696 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.655 |
MOD_GlcNHglycan | 44 | 48 | PF01048 | 0.645 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.723 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.646 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.353 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.681 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.576 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.731 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.734 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.761 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.608 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.709 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.734 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.467 |
MOD_N-GLC_1 | 515 | 520 | PF02516 | 0.568 |
MOD_N-GLC_2 | 54 | 56 | PF02516 | 0.559 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.621 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.581 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.601 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.376 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.517 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.645 |
MOD_NEK2_2 | 132 | 137 | PF00069 | 0.713 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.675 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.429 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.488 |
MOD_PKA_1 | 320 | 326 | PF00069 | 0.779 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.463 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.731 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.742 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.662 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.690 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.681 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.467 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.373 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.618 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.584 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.658 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.572 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.624 |
MOD_Plk_2-3 | 588 | 594 | PF00069 | 0.418 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.692 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.708 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.725 |
MOD_Plk_4 | 503 | 509 | PF00069 | 0.717 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.525 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.640 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.747 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.701 |
MOD_SUMO_rev_2 | 531 | 539 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 569 | 578 | PF00179 | 0.376 |
TRG_DiLeu_BaEn_1 | 517 | 522 | PF01217 | 0.625 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.684 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.639 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.775 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.704 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.577 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 631 | 634 | PF00400 | 0.552 |
TRG_NLS_Bipartite_1 | 159 | 174 | PF00514 | 0.574 |
TRG_NLS_MonoCore_2 | 169 | 174 | PF00514 | 0.700 |
TRG_NLS_MonoExtC_3 | 631 | 636 | PF00514 | 0.566 |
TRG_NLS_MonoExtN_4 | 167 | 174 | PF00514 | 0.693 |
TRG_NLS_MonoExtN_4 | 358 | 365 | PF00514 | 0.471 |
TRG_NLS_MonoExtN_4 | 629 | 636 | PF00514 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.701 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB00 | Leptomonas seymouri | 55% | 100% |
A0A3Q8ICH7 | Leishmania donovani | 90% | 91% |
A4H8I6 | Leishmania braziliensis | 81% | 100% |
A4HWW3 | Leishmania infantum | 90% | 91% |
C9ZPQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QEV5 | Leishmania major | 88% | 100% |