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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X2F1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
GO:0106310 | protein serine kinase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.832 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.832 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.429 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.765 |
DOC_CKS1_1 | 330 | 335 | PF01111 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 546 | 552 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 316 | 326 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 387 | 396 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 296 | 302 | PF00149 | 0.505 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.608 |
DOC_PP4_FxxP_1 | 330 | 333 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.544 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 136 | 146 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 325 | 330 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.505 |
LIG_APCC_ABBA_1 | 43 | 48 | PF00400 | 0.665 |
LIG_APCC_ABBAyCdc20_2 | 42 | 48 | PF00400 | 0.667 |
LIG_BIR_III_4 | 397 | 401 | PF00653 | 0.344 |
LIG_CtBP_PxDLS_1 | 516 | 520 | PF00389 | 0.505 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.753 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.737 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.505 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.399 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.330 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.505 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.505 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.407 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 328 | 333 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 406 | 412 | PF02991 | 0.407 |
LIG_LIR_Apic_2 | 463 | 469 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.780 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.353 |
LIG_LYPXL_yS_3 | 208 | 211 | PF13949 | 0.666 |
LIG_MAD2 | 219 | 227 | PF02301 | 0.657 |
LIG_NRP_CendR_1 | 585 | 587 | PF00754 | 0.508 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 510 | 513 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.381 |
LIG_SH3_2 | 247 | 252 | PF14604 | 0.663 |
LIG_SH3_2 | 416 | 421 | PF14604 | 0.330 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.743 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.785 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.700 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.505 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.715 |
LIG_SUMO_SIM_anti_2 | 334 | 341 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 547 | 553 | PF11976 | 0.501 |
LIG_TRAF2_1 | 573 | 576 | PF00917 | 0.291 |
LIG_UBA3_1 | 559 | 566 | PF00899 | 0.505 |
LIG_WW_1 | 498 | 501 | PF00397 | 0.505 |
LIG_WW_2 | 68 | 71 | PF00397 | 0.680 |
MOD_CDC14_SPxK_1 | 133 | 136 | PF00782 | 0.664 |
MOD_CDC14_SPxK_1 | 22 | 25 | PF00782 | 0.834 |
MOD_CDK_SPxK_1 | 130 | 136 | PF00069 | 0.668 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.837 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.692 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.714 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.723 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.631 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.487 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.514 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.468 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.563 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.505 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.505 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.505 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.451 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.364 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.448 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.793 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.435 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.407 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.466 |
MOD_Cter_Amidation | 455 | 458 | PF01082 | 0.505 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.760 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.776 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.732 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.734 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.540 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.535 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.708 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.667 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.506 |
MOD_GlcNHglycan | 239 | 243 | PF01048 | 0.605 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.505 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.505 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.504 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.210 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.395 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.338 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.437 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.191 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.675 |
MOD_GlcNHglycan | 567 | 571 | PF01048 | 0.388 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.558 |
MOD_GlcNHglycan | 81 | 86 | PF01048 | 0.645 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.777 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.502 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.799 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.708 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.662 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.536 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.631 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.505 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.395 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.427 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.505 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.505 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.442 |
MOD_LATS_1 | 181 | 187 | PF00433 | 0.734 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.381 |
MOD_N-GLC_2 | 541 | 543 | PF02516 | 0.330 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.821 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.713 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.584 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.749 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.790 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.505 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.375 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.425 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.427 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.805 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.505 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.505 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.372 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.505 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.466 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.695 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.505 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.785 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.344 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.420 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.198 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.498 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.403 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.707 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.662 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.800 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.665 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.771 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.505 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.505 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.427 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.786 |
MOD_SUMO_for_1 | 389 | 392 | PF00179 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.799 |
TRG_DiLeu_BaLyEn_6 | 8 | 13 | PF01217 | 0.811 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.666 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.772 |
TRG_Pf-PMV_PEXEL_1 | 302 | 307 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 387 | 392 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8INQ4 | Leishmania donovani | 26% | 100% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A4H459 | Leishmania braziliensis | 27% | 100% |
A4HD79 | Leishmania braziliensis | 27% | 100% |
A4HED7 | Leishmania braziliensis | 28% | 100% |
A4HHE4 | Leishmania braziliensis | 74% | 100% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4I1T4 | Leishmania infantum | 26% | 100% |
E9ADZ1 | Leishmania major | 92% | 100% |
E9AHI7 | Leishmania infantum | 99% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ALU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AXW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q09170 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
Q4Q9K2 | Leishmania major | 27% | 100% |
Q4QJJ0 | Leishmania major | 26% | 100% |
Q5MPA9 | Rattus norvegicus | 28% | 77% |
V5BFI8 | Trypanosoma cruzi | 25% | 100% |