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:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4H8I6
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 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0018193 | peptidyl-amino acid modification | 5 | 3 |
GO:0018208 | peptidyl-proline modification | 6 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0036211 | protein modification process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016853 | isomerase activity | 2 | 10 |
GO:0016859 | cis-trans isomerase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.740 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.529 |
CLV_PCSK_FUR_1 | 273 | 277 | PF00082 | 0.734 |
CLV_PCSK_FUR_1 | 318 | 322 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 630 | 632 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 167 | 173 | PF00082 | 0.696 |
CLV_PCSK_PC7_1 | 626 | 632 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.610 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.719 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.789 |
DEG_SPOP_SBC_1 | 215 | 219 | PF00917 | 0.536 |
DEG_SPOP_SBC_1 | 439 | 443 | PF00917 | 0.538 |
DOC_CYCLIN_RxL_1 | 83 | 90 | PF00134 | 0.692 |
DOC_MAPK_gen_1 | 626 | 636 | PF00069 | 0.683 |
DOC_MAPK_MEF2A_6 | 227 | 235 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 256 | 263 | PF00069 | 0.697 |
DOC_MAPK_MEF2A_6 | 425 | 434 | PF00069 | 0.768 |
DOC_MAPK_MEF2A_6 | 511 | 520 | PF00069 | 0.652 |
DOC_MAPK_RevD_3 | 306 | 321 | PF00069 | 0.750 |
DOC_PP2B_PxIxI_1 | 429 | 435 | PF00149 | 0.779 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.718 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 181 | 191 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 405 | 415 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 500 | 505 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 563 | 571 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 576 | 580 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 257 | 274 | PF00022 | 0.637 |
LIG_BIR_III_2 | 124 | 128 | PF00653 | 0.685 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.698 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.702 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.677 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.600 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.561 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.552 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.644 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.722 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.790 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.481 |
LIG_Integrin_RGD_1 | 530 | 532 | PF01839 | 0.699 |
LIG_LIR_Apic_2 | 309 | 313 | PF02991 | 0.689 |
LIG_LIR_Apic_2 | 339 | 345 | PF02991 | 0.481 |
LIG_LIR_Apic_2 | 413 | 418 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 32 | 43 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 49 | 60 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 585 | 593 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 585 | 589 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.550 |
LIG_PTB_Apo_2 | 456 | 463 | PF02174 | 0.613 |
LIG_PTB_Phospho_1 | 456 | 462 | PF10480 | 0.669 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.755 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.497 |
LIG_SH2_PTP2 | 195 | 198 | PF00017 | 0.533 |
LIG_SH2_PTP2 | 258 | 261 | PF00017 | 0.671 |
LIG_SH2_PTP2 | 333 | 336 | PF00017 | 0.729 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.745 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.780 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.749 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.625 |
LIG_SH3_1 | 332 | 338 | PF00018 | 0.484 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.545 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.704 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.489 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.734 |
LIG_SUMO_SIM_anti_2 | 452 | 458 | PF11976 | 0.656 |
LIG_SUMO_SIM_anti_2 | 514 | 520 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.453 |
LIG_TYR_ITIM | 579 | 584 | PF00017 | 0.344 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.769 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.618 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.604 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.590 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.716 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.764 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.672 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.583 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.622 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.670 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.777 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.781 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.369 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.594 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.690 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.559 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.593 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.718 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.738 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.592 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.530 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.665 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.597 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.544 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.770 |
MOD_GlcNHglycan | 44 | 48 | PF01048 | 0.662 |
MOD_GlcNHglycan | 446 | 450 | PF01048 | 0.618 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.749 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.649 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.353 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.684 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.627 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.751 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.715 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.557 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.782 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.552 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.641 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.659 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.658 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.600 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.435 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.616 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.550 |
MOD_N-GLC_2 | 54 | 56 | PF02516 | 0.523 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.601 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.595 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.589 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.344 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.468 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.543 |
MOD_NEK2_2 | 410 | 415 | PF00069 | 0.712 |
MOD_PIKK_1 | 556 | 562 | PF00454 | 0.369 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.441 |
MOD_PKA_1 | 320 | 326 | PF00069 | 0.757 |
MOD_PKA_1 | 500 | 506 | PF00069 | 0.718 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.687 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.590 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.658 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.602 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.299 |
MOD_PKB_1 | 318 | 326 | PF00069 | 0.616 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.616 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.602 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.696 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.571 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.649 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.678 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.642 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.644 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.663 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.546 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.669 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.730 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.503 |
MOD_SUMO_rev_2 | 528 | 536 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 566 | 575 | PF00179 | 0.344 |
TRG_DiLeu_BaEn_1 | 514 | 519 | PF01217 | 0.578 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.755 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.671 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.713 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.743 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 317 | 320 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.511 |
TRG_NLS_MonoCore_2 | 169 | 174 | PF00514 | 0.702 |
TRG_NLS_MonoExtC_3 | 116 | 122 | PF00514 | 0.638 |
TRG_NLS_MonoExtC_3 | 628 | 633 | PF00514 | 0.479 |
TRG_NLS_MonoExtN_4 | 116 | 121 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 167 | 174 | PF00514 | 0.696 |
TRG_NLS_MonoExtN_4 | 626 | 633 | PF00514 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 495 | 499 | PF00026 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 601 | 605 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB00 | Leptomonas seymouri | 55% | 100% |
A0A3Q8ICH7 | Leishmania donovani | 81% | 91% |
A0A422MVZ8 | Trypanosoma rangeli | 35% | 100% |
A4HWW3 | Leishmania infantum | 80% | 91% |
C9ZPQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AQM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QEV5 | Leishmania major | 78% | 100% |
V5DDE8 | Trypanosoma cruzi | 35% | 100% |