Homologous to other eukaryotic P-type Ca2+ ATPases.. For some reason, this group has heavily expanded in Kinetoplastida.. Localization: Endosomal (by homology) / ER (by homology)
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4H516
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 3 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005215 | transporter activity | 1 | 3 |
GO:0005388 | P-type calcium transporter activity | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 3 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 3 |
GO:0015662 | P-type ion transporter activity | 4 | 3 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.805 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.492 |
DOC_CYCLIN_RxL_1 | 293 | 303 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 295 | 302 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 370 | 376 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 295 | 304 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 443 | 450 | PF00069 | 0.500 |
DOC_MAPK_NFAT4_5 | 221 | 229 | PF00069 | 0.500 |
DOC_MAPK_NFAT4_5 | 295 | 303 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 280 | 287 | PF00149 | 0.545 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.625 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.542 |
LIG_APCC_ABBA_1 | 462 | 467 | PF00400 | 0.408 |
LIG_APCC_ABBAyCdc20_2 | 541 | 547 | PF00400 | 0.701 |
LIG_BIR_III_4 | 192 | 196 | PF00653 | 0.625 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.408 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.491 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.454 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.300 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.672 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.625 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.625 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.633 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.646 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.579 |
LIG_IBAR_NPY_1 | 173 | 175 | PF08397 | 0.625 |
LIG_KLC1_Yacidic_2 | 542 | 547 | PF13176 | 0.695 |
LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 410 | 421 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 432 | 441 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 467 | 474 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 185 | 189 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.371 |
LIG_NRBOX | 436 | 442 | PF00104 | 0.542 |
LIG_PCNA_yPIPBox_3 | 288 | 298 | PF02747 | 0.535 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.381 |
LIG_Pex14_2 | 506 | 510 | PF04695 | 0.605 |
LIG_PTB_Apo_2 | 170 | 177 | PF02174 | 0.625 |
LIG_PTB_Apo_2 | 185 | 192 | PF02174 | 0.438 |
LIG_PTB_Apo_2 | 249 | 256 | PF02174 | 0.538 |
LIG_PTB_Apo_2 | 392 | 399 | PF02174 | 0.342 |
LIG_PTB_Phospho_1 | 170 | 176 | PF10480 | 0.625 |
LIG_PTB_Phospho_1 | 185 | 191 | PF10480 | 0.438 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.700 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 67 | 70 | PF00017 | 0.707 |
LIG_SH2_PTP2 | 306 | 309 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.657 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.575 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 269 | 275 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 233 | 238 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 269 | 275 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 458 | 463 | PF11976 | 0.408 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.525 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.575 |
LIG_TRAF2_1 | 536 | 539 | PF00917 | 0.642 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.598 |
LIG_TYR_ITIM | 304 | 309 | PF00017 | 0.525 |
LIG_UBA3_1 | 421 | 429 | PF00899 | 0.315 |
LIG_WRC_WIRS_1 | 450 | 455 | PF05994 | 0.525 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.394 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.408 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.465 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.525 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.558 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.457 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.559 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.434 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.430 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.350 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.350 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.350 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.468 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.350 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.525 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.543 |
MOD_LATS_1 | 52 | 58 | PF00433 | 0.525 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.458 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.596 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.387 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.350 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.350 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.350 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.350 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.350 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.350 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.408 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.350 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.663 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.668 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.514 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.525 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.350 |
MOD_PKA_1 | 36 | 42 | PF00069 | 0.350 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.350 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.552 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.525 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.669 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.596 |
MOD_Plk_2-3 | 349 | 355 | PF00069 | 0.525 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.356 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.381 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.369 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.401 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.350 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.350 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.525 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.531 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.350 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.408 |
MOD_SUMO_rev_2 | 3 | 11 | PF00179 | 0.552 |
MOD_SUMO_rev_2 | 33 | 38 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 513 | 522 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_1 | 45 | 50 | PF01217 | 0.525 |
TRG_DiLeu_BaEn_4 | 432 | 438 | PF01217 | 0.408 |
TRG_DiLeu_BaEn_4 | 584 | 590 | PF01217 | 0.716 |
TRG_DiLeu_BaLyEn_6 | 494 | 499 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.434 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.543 |
TRG_NES_CRM1_1 | 119 | 131 | PF08389 | 0.525 |
TRG_NES_CRM1_1 | 217 | 233 | PF08389 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 187 | 192 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 555 | 560 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HT82 | Leishmania infantum | 89% | 69% |
O34431 | Bacillus subtilis (strain 168) | 33% | 67% |
P28877 | Candida albicans | 24% | 66% |
P47317 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 30% | 68% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 31% | 67% |
Q9CFU9 | Lactococcus lactis subsp. lactis (strain IL1403) | 30% | 67% |