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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q7K3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0106310 | protein serine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 466 | 470 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.596 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.673 |
CLV_PCSK_FUR_1 | 451 | 455 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.167 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.391 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.651 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.515 |
DOC_CKS1_1 | 565 | 570 | PF01111 | 0.737 |
DOC_CYCLIN_RxL_1 | 184 | 193 | PF00134 | 0.515 |
DOC_CYCLIN_RxL_1 | 400 | 410 | PF00134 | 0.218 |
DOC_MAPK_gen_1 | 216 | 225 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 290 | 297 | PF00069 | 0.621 |
DOC_MAPK_JIP1_4 | 20 | 26 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 370 | 379 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 46 | 55 | PF00069 | 0.486 |
DOC_PP1_RVXF_1 | 185 | 192 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 374 | 380 | PF00149 | 0.422 |
DOC_PP4_FxxP_1 | 512 | 515 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.721 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.663 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 523 | 531 | PF00244 | 0.631 |
LIG_Actin_WH2_2 | 33 | 48 | PF00022 | 0.502 |
LIG_APCC_ABBA_1 | 415 | 420 | PF00400 | 0.468 |
LIG_APCC_ABBA_1 | 509 | 514 | PF00400 | 0.462 |
LIG_APCC_ABBAyCdc20_2 | 414 | 420 | PF00400 | 0.374 |
LIG_BIR_III_2 | 527 | 531 | PF00653 | 0.538 |
LIG_BIR_III_4 | 382 | 386 | PF00653 | 0.374 |
LIG_BIR_III_4 | 480 | 484 | PF00653 | 0.595 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 324 | 334 | PF00928 | 0.362 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.455 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.464 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.726 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.452 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.253 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.707 |
LIG_FXI_DFP_1 | 233 | 237 | PF00024 | 0.252 |
LIG_LIR_Apic_2 | 313 | 319 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 505 | 515 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 514 | 520 | PF02991 | 0.333 |
LIG_PCNA_yPIPBox_3 | 62 | 75 | PF02747 | 0.538 |
LIG_Pex14_2 | 105 | 109 | PF04695 | 0.557 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 341 | 345 | PF00017 | 0.362 |
LIG_SH2_PTP2 | 316 | 319 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 517 | 521 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.500 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.405 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.572 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.497 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.726 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.637 |
LIG_SUMO_SIM_par_1 | 201 | 206 | PF11976 | 0.530 |
LIG_SxIP_EBH_1 | 174 | 185 | PF03271 | 0.557 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.518 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.339 |
LIG_WRC_WIRS_1 | 447 | 452 | PF05994 | 0.541 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.514 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.519 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.649 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.305 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.423 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.675 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.611 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.443 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.425 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.425 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.549 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.708 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.436 |
MOD_Cter_Amidation | 392 | 395 | PF01082 | 0.257 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.332 |
MOD_GlcNHglycan | 165 | 169 | PF01048 | 0.335 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.619 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.281 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.358 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.665 |
MOD_GlcNHglycan | 480 | 484 | PF01048 | 0.672 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.580 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.696 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.613 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.471 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.491 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.609 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.443 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.476 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.615 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.647 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.677 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.438 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.636 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.766 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.524 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.287 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.423 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.632 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.733 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.444 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.651 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.509 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.405 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.605 |
MOD_PK_1 | 70 | 76 | PF00069 | 0.538 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.539 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.553 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.275 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.539 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.551 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.321 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.608 |
MOD_PKB_1 | 291 | 299 | PF00069 | 0.689 |
MOD_PKB_1 | 304 | 312 | PF00069 | 0.394 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.426 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.707 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.374 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.733 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.531 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.530 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.305 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.663 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 218 | 221 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 318 | 328 | PF00179 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 402 | 407 | PF01217 | 0.218 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.437 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.600 |
TRG_NES_CRM1_1 | 193 | 206 | PF08389 | 0.530 |
TRG_NES_CRM1_1 | 347 | 360 | PF08389 | 0.257 |
TRG_Pf-PMV_PEXEL_1 | 216 | 221 | PF00026 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 405 | 410 | PF00026 | 0.218 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMI5 | Leptomonas seymouri | 57% | 99% |
A0A0S4IZ51 | Bodo saltans | 39% | 100% |
A0A1X0P290 | Trypanosomatidae | 45% | 100% |
A0A3S7X363 | Leishmania donovani | 94% | 100% |
A0A422P4X7 | Trypanosoma rangeli | 40% | 100% |
A4HI55 | Leishmania braziliensis | 77% | 100% |
A4I5D1 | Leishmania infantum | 94% | 100% |
C9ZQR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9B0M9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q94E49 | Oryza sativa subsp. japonica | 24% | 100% |
V5BU83 | Trypanosoma cruzi | 41% | 100% |