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. | yes | yes: 10 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031588 | nucleotide-activated protein kinase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902911 | protein kinase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9B5V6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0007154 | cell communication | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009267 | cellular response to starvation | 4 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0009991 | response to extracellular stimulus | 3 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031667 | response to nutrient levels | 4 | 1 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 1 |
GO:0031669 | cellular response to nutrient levels | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0042149 | cellular response to glucose starvation | 5 | 1 |
GO:0042594 | response to starvation | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071496 | cellular response to external stimulus | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016208 | AMP binding | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0019207 | kinase regulator activity | 3 | 1 |
GO:0019887 | protein kinase regulator activity | 4 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0019900 | kinase binding | 4 | 1 |
GO:0019901 | protein kinase binding | 5 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 232 | 236 | PF00656 | 0.820 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.625 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 95 | 97 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 397 | 405 | PF00400 | 0.495 |
DEG_SCF_TRCP1_1 | 266 | 271 | PF00400 | 0.561 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.467 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.785 |
DOC_CYCLIN_RxL_1 | 446 | 456 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 94 | 101 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 366 | 375 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 388 | 395 | PF00069 | 0.452 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.764 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.480 |
DOC_PP4_FxxP_1 | 341 | 344 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.847 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.498 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 50 | 58 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.556 |
LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.500 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BIR_III_4 | 235 | 239 | PF00653 | 0.773 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.855 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.510 |
LIG_CaM_IQ_9 | 409 | 425 | PF13499 | 0.606 |
LIG_Clathr_ClatBox_1 | 401 | 405 | PF01394 | 0.497 |
LIG_Clathr_ClatBox_1 | 452 | 456 | PF01394 | 0.420 |
LIG_EH1_1 | 176 | 184 | PF00400 | 0.451 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.398 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.693 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.460 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.477 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.465 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.483 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.531 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.595 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.600 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.443 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.539 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.625 |
LIG_LIR_Apic_2 | 338 | 344 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 130 | 138 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 342 | 353 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.814 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.455 |
LIG_PCNA_yPIPBox_3 | 461 | 472 | PF02747 | 0.419 |
LIG_Pex14_2 | 341 | 345 | PF04695 | 0.483 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.472 |
LIG_SH2_CRK | 55 | 59 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 337 | 341 | PF00017 | 0.550 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.363 |
LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.579 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 410 | 413 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.484 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.716 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.660 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.517 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.484 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 368 | 376 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 61 | 68 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 181 | 187 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 371 | 376 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.199 |
LIG_SUMO_SIM_par_1 | 61 | 68 | PF11976 | 0.467 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.549 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.463 |
LIG_TRFH_1 | 302 | 306 | PF08558 | 0.605 |
LIG_TYR_ITIM | 205 | 210 | PF00017 | 0.530 |
LIG_TYR_ITSM | 103 | 110 | PF00017 | 0.413 |
LIG_UBA3_1 | 182 | 188 | PF00899 | 0.452 |
LIG_UBA3_1 | 211 | 217 | PF00899 | 0.566 |
LIG_UBA3_1 | 359 | 366 | PF00899 | 0.530 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.493 |
MOD_CDK_SPK_2 | 383 | 388 | PF00069 | 0.452 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.788 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.834 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.575 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.578 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.625 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.507 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.570 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.452 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.474 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.548 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.682 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.530 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.668 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.624 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.730 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.704 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.573 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.687 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.780 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.693 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.476 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.579 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.785 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.764 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.553 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.808 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.494 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.545 |
MOD_NEK2_2 | 336 | 341 | PF00069 | 0.543 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.618 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.579 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.484 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.630 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.428 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.405 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.800 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.553 |
MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.548 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.697 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.559 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.580 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.497 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.498 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.630 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.787 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.452 |
TRG_AP2beta_CARGO_1 | 439 | 448 | PF09066 | 0.433 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_2 | 469 | 475 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_4 | 36 | 42 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 458 | 463 | PF01217 | 0.572 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 93 | 96 | PF00400 | 0.632 |
TRG_NES_CRM1_1 | 56 | 68 | PF08389 | 0.536 |
TRG_NLS_MonoExtN_4 | 93 | 98 | PF00514 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 461 | 465 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCX9 | Leptomonas seymouri | 75% | 99% |
A0A1X0NKG9 | Trypanosomatidae | 44% | 90% |
A0A3Q8ILV4 | Leishmania donovani | 96% | 100% |
A0A422NI77 | Trypanosoma rangeli | 48% | 96% |
A4HMA8 | Leishmania braziliensis | 83% | 99% |
A4IAX4 | Leishmania infantum | 96% | 100% |
D0A281 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 96% |
E9AEQ1 | Leishmania major | 95% | 100% |
V5BSS4 | Trypanosoma cruzi | 50% | 96% |