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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H848
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004713 | protein tyrosine kinase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.560 |
CLV_MEL_PAP_1 | 422 | 428 | PF00089 | 0.543 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.678 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.227 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.335 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.522 |
DEG_APCC_KENBOX_2 | 293 | 297 | PF00400 | 0.480 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.742 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.649 |
DOC_CKS1_1 | 531 | 536 | PF01111 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 53 | 59 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 194 | 203 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 283 | 292 | PF00069 | 0.227 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.414 |
DOC_PP4_FxxP_1 | 249 | 252 | PF00568 | 0.378 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.707 |
DOC_PP4_FxxP_1 | 548 | 551 | PF00568 | 0.597 |
DOC_PP4_FxxP_1 | 640 | 643 | PF00568 | 0.755 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.323 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.443 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.543 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 18 | 26 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 380 | 386 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 477 | 481 | PF00244 | 0.545 |
LIG_AP2alpha_1 | 507 | 511 | PF02296 | 0.648 |
LIG_AP2alpha_1 | 669 | 673 | PF02296 | 0.662 |
LIG_AP2alpha_2 | 256 | 258 | PF02296 | 0.447 |
LIG_AP2alpha_2 | 667 | 669 | PF02296 | 0.606 |
LIG_APCC_ABBAyCdc20_2 | 503 | 509 | PF00400 | 0.593 |
LIG_BIR_III_2 | 488 | 492 | PF00653 | 0.544 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 636 | 640 | PF00533 | 0.685 |
LIG_BRCT_BRCA1_2 | 288 | 294 | PF00533 | 0.392 |
LIG_deltaCOP1_diTrp_1 | 326 | 332 | PF00928 | 0.298 |
LIG_deltaCOP1_diTrp_1 | 357 | 362 | PF00928 | 0.570 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.351 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.464 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.380 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.322 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.652 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.583 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.447 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.447 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.586 |
LIG_IBAR_NPY_1 | 564 | 566 | PF08397 | 0.536 |
LIG_LIR_Apic_2 | 246 | 252 | PF02991 | 0.237 |
LIG_LIR_Apic_2 | 382 | 386 | PF02991 | 0.778 |
LIG_LIR_Apic_2 | 411 | 417 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 508 | 514 | PF02991 | 0.709 |
LIG_LIR_Apic_2 | 546 | 551 | PF02991 | 0.603 |
LIG_LIR_Apic_2 | 637 | 643 | PF02991 | 0.756 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 505 | 514 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 667 | 673 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 667 | 672 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.355 |
LIG_LRP6_Inhibitor_1 | 333 | 339 | PF00058 | 0.287 |
LIG_MAD2 | 368 | 376 | PF02301 | 0.641 |
LIG_MYND_1 | 516 | 520 | PF01753 | 0.540 |
LIG_NRBOX | 316 | 322 | PF00104 | 0.281 |
LIG_Pex14_1 | 297 | 301 | PF04695 | 0.545 |
LIG_Pex14_2 | 507 | 511 | PF04695 | 0.648 |
LIG_Pex14_2 | 669 | 673 | PF04695 | 0.619 |
LIG_PTAP_UEV_1 | 526 | 531 | PF05743 | 0.771 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.378 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.529 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.529 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.790 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.529 |
LIG_SH2_NCK_1 | 614 | 618 | PF00017 | 0.754 |
LIG_SH2_PTP2 | 74 | 77 | PF00017 | 0.355 |
LIG_SH2_SRC | 414 | 417 | PF00017 | 0.531 |
LIG_SH2_SRC | 614 | 617 | PF00017 | 0.786 |
LIG_SH2_STAT3 | 455 | 458 | PF00017 | 0.651 |
LIG_SH2_STAT3 | 593 | 596 | PF00017 | 0.794 |
LIG_SH2_STAT3 | 626 | 629 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.355 |
LIG_SH3_2 | 661 | 666 | PF14604 | 0.603 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.447 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.630 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.660 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.760 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.683 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.630 |
LIG_SH3_3 | 610 | 616 | PF00018 | 0.703 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.631 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 109 | 114 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 34 | 41 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 436 | 444 | PF11976 | 0.499 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.447 |
LIG_TRAF2_1 | 433 | 436 | PF00917 | 0.719 |
LIG_TRAF2_1 | 617 | 620 | PF00917 | 0.550 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.504 |
LIG_WW_1 | 54 | 57 | PF00397 | 0.613 |
MOD_CDC14_SPxK_1 | 385 | 388 | PF00782 | 0.525 |
MOD_CDC14_SPxK_1 | 663 | 666 | PF00782 | 0.538 |
MOD_CDK_SPK_2 | 382 | 387 | PF00069 | 0.649 |
MOD_CDK_SPK_2 | 660 | 665 | PF00069 | 0.543 |
MOD_CDK_SPxK_1 | 382 | 388 | PF00069 | 0.525 |
MOD_CDK_SPxK_1 | 660 | 666 | PF00069 | 0.542 |
MOD_CDK_SPxxK_3 | 243 | 250 | PF00069 | 0.289 |
MOD_CDK_SPxxK_3 | 641 | 648 | PF00069 | 0.546 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.405 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.365 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.441 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.271 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.709 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.659 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.587 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.390 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.447 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.463 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.563 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.378 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.657 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.786 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.667 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.684 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.674 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.686 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.441 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.363 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.227 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.324 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.263 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.532 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.526 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.537 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.752 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.423 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.549 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.334 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.335 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.387 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.564 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.673 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.777 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.378 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.364 |
MOD_NEK2_2 | 418 | 423 | PF00069 | 0.679 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.324 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.618 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.330 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.451 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.359 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.680 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.726 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.637 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.486 |
MOD_PKB_1 | 152 | 160 | PF00069 | 0.289 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.454 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.452 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.737 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.355 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.289 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.670 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.700 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.787 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.693 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.539 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.546 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.542 |
MOD_SUMO_for_1 | 470 | 473 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 498 | 506 | PF00179 | 0.770 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 150 | 152 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 422 | 425 | PF00400 | 0.688 |
TRG_NLS_MonoExtC_3 | 259 | 265 | PF00514 | 0.447 |
TRG_NLS_MonoExtN_4 | 257 | 264 | PF00514 | 0.447 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7R8 | Leptomonas seymouri | 60% | 96% |
A0A1X0NUC1 | Trypanosomatidae | 46% | 89% |
A0A3S7WTG9 | Leishmania donovani | 67% | 100% |
A0A422NRC0 | Trypanosoma rangeli | 40% | 99% |
A4HWH3 | Leishmania infantum | 67% | 100% |
C9ZXX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AQ75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4QFA8 | Leishmania major | 65% | 96% |
V5BK24 | Trypanosoma cruzi | 42% | 99% |