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:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q2N5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008610 | lipid biosynthetic process | 4 | 2 |
GO:0008654 | phospholipid biosynthetic process | 5 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 2 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 2 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016307 | phosphatidylinositol phosphate kinase activity | 5 | 11 |
GO:0016308 | 1-phosphatidylinositol-4-phosphate 5-kinase activity | 6 | 3 |
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:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.132 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.455 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.191 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.240 |
CLV_PCSK_FUR_1 | 184 | 188 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.310 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 4 | 12 | PF00400 | 0.675 |
DEG_APCC_DBOX_1 | 507 | 515 | PF00400 | 0.302 |
DEG_SCF_FBW7_1 | 255 | 261 | PF00400 | 0.260 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.453 |
DOC_CKS1_1 | 255 | 260 | PF01111 | 0.336 |
DOC_CYCLIN_RxL_1 | 2 | 10 | PF00134 | 0.667 |
DOC_PP1_RVXF_1 | 534 | 541 | PF00149 | 0.257 |
DOC_PP4_FxxP_1 | 178 | 181 | PF00568 | 0.631 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.257 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.283 |
DOC_USP7_UBL2_3 | 338 | 342 | PF12436 | 0.261 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.262 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 356 | 361 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 430 | 437 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 472 | 481 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 522 | 530 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 70 | 78 | PF00244 | 0.528 |
LIG_Actin_WH2_1 | 270 | 288 | PF00022 | 0.371 |
LIG_Actin_WH2_2 | 301 | 316 | PF00022 | 0.340 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.369 |
LIG_EH_1 | 298 | 302 | PF12763 | 0.340 |
LIG_EVH1_2 | 215 | 219 | PF00568 | 0.545 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.394 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.340 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.420 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.695 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.402 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.283 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.319 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.324 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.428 |
LIG_LIR_Gen_1 | 195 | 205 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 250 | 258 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 319 | 330 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 399 | 408 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.257 |
LIG_PDZ_Class_2 | 541 | 546 | PF00595 | 0.257 |
LIG_Pex14_1 | 516 | 520 | PF04695 | 0.292 |
LIG_REV1ctd_RIR_1 | 264 | 274 | PF16727 | 0.276 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.485 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.257 |
LIG_SH2_PTP2 | 495 | 498 | PF00017 | 0.257 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.257 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.452 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.451 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.452 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.301 |
LIG_TRFH_1 | 301 | 305 | PF08558 | 0.326 |
LIG_TYR_ITIM | 493 | 498 | PF00017 | 0.257 |
LIG_UBA3_1 | 381 | 387 | PF00899 | 0.299 |
MOD_CDK_SPxK_1 | 254 | 260 | PF00069 | 0.257 |
MOD_CDK_SPxxK_3 | 177 | 184 | PF00069 | 0.458 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.257 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.326 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.406 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.463 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.689 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.285 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.341 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.273 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.580 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.696 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.673 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.258 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.737 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.262 |
MOD_GlcNHglycan | 453 | 457 | PF01048 | 0.384 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.498 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.712 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.677 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.678 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.484 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.264 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.294 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.321 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.316 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.363 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.399 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.437 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.418 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.637 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.513 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.292 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.354 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.158 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.292 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.292 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.283 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.373 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.233 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.258 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.680 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.539 |
MOD_NEK2_2 | 37 | 42 | PF00069 | 0.620 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.664 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.626 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.292 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.277 |
MOD_PK_1 | 251 | 257 | PF00069 | 0.388 |
MOD_PK_1 | 88 | 94 | PF00069 | 0.468 |
MOD_PKA_1 | 355 | 361 | PF00069 | 0.306 |
MOD_PKA_1 | 523 | 529 | PF00069 | 0.282 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.678 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.292 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.391 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.347 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.268 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.716 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.259 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.384 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.664 |
MOD_Plk_2-3 | 200 | 206 | PF00069 | 0.665 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.610 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.268 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.307 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.268 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.457 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.292 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.262 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.391 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.683 |
MOD_SUMO_rev_2 | 234 | 242 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 337 | 344 | PF00179 | 0.257 |
MOD_SUMO_rev_2 | 518 | 525 | PF00179 | 0.340 |
TRG_DiLeu_BaEn_1 | 376 | 381 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.257 |
TRG_ER_diArg_1 | 184 | 187 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 522 | 525 | PF00400 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 378 | 383 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCT9 | Leptomonas seymouri | 67% | 100% |
A0A0S4IZA7 | Bodo saltans | 46% | 100% |
A0A1X0P9B0 | Trypanosomatidae | 25% | 100% |
A0A1X0PB79 | Trypanosomatidae | 48% | 100% |
A0A381MTN1 | Leishmania infantum | 95% | 100% |
A0A3Q8ILB5 | Leishmania donovani | 94% | 100% |
A0A422N247 | Trypanosoma rangeli | 45% | 100% |
A4HB28 | Leishmania braziliensis | 77% | 100% |
A4HNP5 | Leishmania braziliensis | 22% | 100% |
E9B598 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
O48709 | Arabidopsis thaliana | 33% | 77% |
Q6EX42 | Oryza sativa subsp. japonica | 29% | 68% |
Q8L850 | Arabidopsis thaliana | 30% | 67% |
Q9LMN1 | Arabidopsis thaliana | 26% | 100% |
Q9M149 | Arabidopsis thaliana | 27% | 100% |
Q9SUI2 | Arabidopsis thaliana | 31% | 72% |
V5BA13 | Trypanosoma cruzi | 28% | 100% |
V5BV28 | Trypanosoma cruzi | 48% | 100% |