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: 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S7X0V1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.431 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.397 |
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.372 |
CLV_TASPASE1 | 495 | 501 | PF01112 | 0.582 |
DEG_APCC_DBOX_1 | 125 | 133 | PF00400 | 0.355 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.348 |
DOC_MAPK_DCC_7 | 126 | 134 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.396 |
DOC_PP4_FxxP_1 | 548 | 551 | PF00568 | 0.658 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.599 |
LIG_14-3-3_CanoR_1 | 105 | 109 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 244 | 248 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 321 | 326 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.320 |
LIG_Actin_WH2_2 | 347 | 362 | PF00022 | 0.279 |
LIG_Actin_WH2_2 | 407 | 422 | PF00022 | 0.391 |
LIG_BIR_III_2 | 532 | 536 | PF00653 | 0.607 |
LIG_BIR_III_4 | 519 | 523 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.329 |
LIG_eIF4E_1 | 344 | 350 | PF01652 | 0.329 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.469 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.370 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.438 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.460 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.615 |
LIG_Integrin_isoDGR_2 | 189 | 191 | PF01839 | 0.517 |
LIG_IRF3_LxIS_1 | 355 | 362 | PF10401 | 0.279 |
LIG_LIR_Gen_1 | 246 | 254 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 319 | 329 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.409 |
LIG_LYPXL_S_1 | 26 | 30 | PF13949 | 0.601 |
LIG_LYPXL_yS_3 | 27 | 30 | PF13949 | 0.600 |
LIG_MYND_1 | 24 | 28 | PF01753 | 0.663 |
LIG_NRBOX | 411 | 417 | PF00104 | 0.384 |
LIG_NRP_CendR_1 | 565 | 568 | PF00754 | 0.606 |
LIG_PCNA_yPIPBox_3 | 213 | 226 | PF02747 | 0.309 |
LIG_Pex14_2 | 102 | 106 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 310 | 317 | PF02174 | 0.373 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.329 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.382 |
LIG_SH2_PTP2 | 344 | 347 | PF00017 | 0.309 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 216 | 219 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 48 | 51 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.471 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.776 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.287 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.632 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.576 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.591 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.633 |
LIG_SUMO_SIM_anti_2 | 223 | 229 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.276 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.483 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.283 |
LIG_UBA3_1 | 177 | 184 | PF00899 | 0.440 |
LIG_WW_1 | 24 | 27 | PF00397 | 0.620 |
MOD_CDK_SPK_2 | 316 | 321 | PF00069 | 0.329 |
MOD_CDK_SPK_2 | 534 | 539 | PF00069 | 0.576 |
MOD_CDK_SPxxK_3 | 558 | 565 | PF00069 | 0.626 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.329 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.682 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.471 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.430 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.620 |
MOD_Cter_Amidation | 189 | 192 | PF01082 | 0.521 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.446 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.567 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.654 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.359 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.731 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.622 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.665 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.370 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.436 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.609 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.570 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.802 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.604 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.628 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.398 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.579 |
MOD_N-GLC_1 | 528 | 533 | PF02516 | 0.647 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.626 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.370 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.329 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.282 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.332 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.444 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.777 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.307 |
MOD_OFUCOSY | 417 | 423 | PF10250 | 0.373 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.811 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.437 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.468 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.329 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.320 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.601 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.649 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.459 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.309 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.368 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.459 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.311 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.376 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.515 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.351 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.740 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.706 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 134 | 137 | PF00179 | 0.415 |
MOD_SUMO_for_1 | 374 | 377 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 149 | 158 | PF00179 | 0.405 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.416 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 306 | 311 | PF01217 | 0.347 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.329 |
TRG_NES_CRM1_1 | 220 | 233 | PF08389 | 0.279 |
TRG_NES_CRM1_1 | 287 | 302 | PF08389 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKB0 | Leptomonas seymouri | 59% | 100% |
A0A0S4IVY6 | Bodo saltans | 29% | 100% |
A0A3Q8ISA0 | Leishmania donovani | 32% | 100% |
A4HFV0 | Leishmania braziliensis | 76% | 98% |
A4HIT6 | Leishmania braziliensis | 31% | 100% |
A4I2Y4 | Leishmania infantum | 100% | 100% |
A4I638 | Leishmania infantum | 32% | 100% |
E9ADF5 | Leishmania major | 94% | 99% |
E9AZ78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B1C3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4Q6U1 | Leishmania major | 31% | 100% |