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 |
Related structures:
AlphaFold database: A4H8Q7
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0007165 | signal transduction | 2 | 11 |
GO:0007186 | G protein-coupled receptor signaling pathway | 3 | 11 |
GO:0007205 | protein kinase C-activating G protein-coupled receptor signaling pathway | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004143 | diacylglycerol kinase activity | 5 | 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:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 322 | 326 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.292 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.381 |
CLV_PCSK_FUR_1 | 138 | 142 | PF00082 | 0.197 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.277 |
DEG_APCC_DBOX_1 | 407 | 415 | PF00400 | 0.348 |
DEG_COP1_1 | 13 | 24 | PF00400 | 0.619 |
DEG_Kelch_Keap1_1 | 80 | 85 | PF01344 | 0.292 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.300 |
DEG_SPOP_SBC_1 | 480 | 484 | PF00917 | 0.197 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.510 |
DOC_CKS1_1 | 494 | 499 | PF01111 | 0.348 |
DOC_CKS1_1 | 542 | 547 | PF01111 | 0.537 |
DOC_CYCLIN_RxL_1 | 437 | 445 | PF00134 | 0.355 |
DOC_MAPK_DCC_7 | 272 | 282 | PF00069 | 0.456 |
DOC_MAPK_DCC_7 | 396 | 406 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 428 | 435 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 578 | 585 | PF00069 | 0.456 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.410 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.297 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.357 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.318 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.694 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 319 | 324 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 423 | 431 | PF00244 | 0.197 |
LIG_14-3-3_CanoR_1 | 578 | 582 | PF00244 | 0.516 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.215 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.433 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.489 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.216 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.292 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.419 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.486 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.279 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.197 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.519 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 463 | 468 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 331 | 337 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 427 | 438 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 535 | 545 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 556 | 563 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 69 | 79 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 331 | 335 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.150 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 58 | 63 | PF02991 | 0.489 |
LIG_MAD2 | 608 | 616 | PF02301 | 0.277 |
LIG_MYND_1 | 208 | 212 | PF01753 | 0.410 |
LIG_PAM2_1 | 229 | 241 | PF00658 | 0.372 |
LIG_PCNA_yPIPBox_3 | 376 | 386 | PF02747 | 0.405 |
LIG_Pex14_2 | 227 | 231 | PF04695 | 0.485 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.288 |
LIG_SH2_CRK | 466 | 470 | PF00017 | 0.410 |
LIG_SH2_CRK | 518 | 522 | PF00017 | 0.410 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.624 |
LIG_SH2_GRB2like | 221 | 224 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 221 | 225 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 558 | 562 | PF00017 | 0.661 |
LIG_SH2_STAP1 | 567 | 571 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.621 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.703 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.373 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.624 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.412 |
LIG_SH3_CIN85_PxpxPR_1 | 493 | 498 | PF14604 | 0.383 |
LIG_SUMO_SIM_anti_2 | 158 | 164 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 498 | 504 | PF11976 | 0.410 |
LIG_TRAF2_2 | 53 | 58 | PF00917 | 0.439 |
LIG_TYR_ITIM | 347 | 352 | PF00017 | 0.297 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.410 |
LIG_TYR_ITIM | 516 | 521 | PF00017 | 0.410 |
MOD_CDC14_SPxK_1 | 132 | 135 | PF00782 | 0.197 |
MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.197 |
MOD_CDK_SPK_2 | 493 | 498 | PF00069 | 0.282 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.282 |
MOD_CDK_SPxxK_3 | 133 | 140 | PF00069 | 0.197 |
MOD_CDK_SPxxK_3 | 229 | 236 | PF00069 | 0.336 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.461 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.621 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.303 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.386 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.228 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.463 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.579 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.357 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.590 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.521 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.597 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.617 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.645 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.513 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.197 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.661 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.397 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.306 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.355 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.613 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.284 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.719 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.197 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.276 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.342 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.439 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.587 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.234 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.363 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.546 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.593 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.339 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.393 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.228 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.329 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.287 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.355 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.577 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.313 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.414 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.410 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.216 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.347 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.173 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.577 |
MOD_PK_1 | 319 | 325 | PF00069 | 0.334 |
MOD_PK_1 | 614 | 620 | PF00069 | 0.529 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.239 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.656 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.279 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.265 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.270 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.519 |
MOD_PKB_1 | 138 | 146 | PF00069 | 0.197 |
MOD_PKB_1 | 612 | 620 | PF00069 | 0.514 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.355 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.211 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.447 |
MOD_Plk_1 | 594 | 600 | PF00069 | 0.464 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.485 |
MOD_Plk_2-3 | 14 | 20 | PF00069 | 0.588 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.719 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.302 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.346 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.197 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.442 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.458 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.529 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.282 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.422 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.571 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.631 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.560 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.324 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.461 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.491 |
TRG_DiLeu_BaEn_2 | 169 | 175 | PF01217 | 0.402 |
TRG_DiLeu_BaEn_2 | 535 | 541 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 117 | 122 | PF01217 | 0.362 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.624 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.197 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 611 | 614 | PF00400 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 120 | 125 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 165 | 170 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRI7 | Leptomonas seymouri | 52% | 83% |
A0A0S4JFM6 | Bodo saltans | 26% | 79% |
A0A3Q8IAN3 | Leishmania donovani | 72% | 85% |
A0A3R7MJ80 | Trypanosoma rangeli | 33% | 94% |
A4HX26 | Leishmania infantum | 72% | 85% |
C9ZVX0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AQU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 85% |
Q4QEN8 | Leishmania major | 70% | 100% |
V5DJ39 | Trypanosoma cruzi | 31% | 94% |