Alignments for a candidate for pccA in Herbaspirillum seropedicae SmR1

GapMind for catabolism of small carbon sources

Alignments for a candidate for pccA in Herbaspirillum seropedicae SmR1

Align Propionyl-CoA carboxylase alpha chain; EC 6.4.1.3 (characterized)
to candidate HSERO_RS23460 HSERO_RS23460 3-methylcrotonyl-CoA carboxylase subunit alpha

Query= SwissProt::Q5LUF3
         (681 letters)



>FitnessBrowser__HerbieS:HSERO_RS23460
          Length = 671

 Score =  525 bits (1351), Expect = e-153
 Identities = 307/695 (44%), Positives = 415/695 (59%), Gaps = 40/695 (5%)

Query: 1   MFNKILIANRGEIACRVIKTARKMGISTVAIYSDADKQALHVQMADEAVHIGPPPANQSY 60
           MF KILIANRGEIACRV  TAR++GI+TVA+YSDAD +A HV   DE+V +GP PA +SY
Sbjct: 1   MFTKILIANRGEIACRVAATARRLGIATVAVYSDADARAKHVAACDESVRLGPAPARESY 60

Query: 61  IVIDKVMAAIRATGAQAVHPGYGFLSENSKFAEALEAEGVIFVGPPKGAIEAMGDKITSK 120
           +  +K++AA  ATGAQA+HPGYGFLSEN+ FA+A    G++F+GPP  AIEAMG K  +K
Sbjct: 61  LCAEKIIAAALATGAQAIHPGYGFLSENAGFAQACAQAGLVFIGPPASAIEAMGSKAAAK 120

Query: 121 KIAQEANVSTVPGYMGLIEDADEAVKISNQIGYPVMIKASAGGGGKGMRIAWNDQEAREG 180
            + ++A V  VPGY G  +++      +++IGYPV++KASAGGGGKGMR+    ++    
Sbjct: 121 ALMEQAAVPLVPGYHGEEQESGLLHSQADRIGYPVLLKASAGGGGKGMRVVERSEDFDAA 180

Query: 181 FQSSKNEAANSFGDDRIFIEKFVTQPRHIEIQVLCDSHGNGIYLGERECSIQRRNQKVVE 240
             S K EA  SFGDDR+ +EK++T+PRHIEIQV  D HG+ +YL ER+CS+QRR+QKV+E
Sbjct: 181 LASCKREAIASFGDDRVLVEKYLTRPRHIEIQVFADGHGHCVYLFERDCSVQRRHQKVLE 240

Query: 241 EAPSPFLDEATRRAMGEQAVALAKAVGYASAGTVEFIVDGQKNFYFLEMNTRLQVEHPVT 300
           EAP+P + E  R AMGE AVA A+AVGY  AGTVEFI +   +FYF+EMNTRLQVEHPVT
Sbjct: 241 EAPAPGMSEERRAAMGEAAVAAARAVGYVGAGTVEFIANQDGSFYFMEMNTRLQVEHPVT 300

Query: 301 ELITGVDLVEQMIRVAAGEPLSITQGDVKLTGWAIENRLYAEDPYRGFLPSIGRLTRYRP 360
           E+ITG+DLVE  +RVAAG+ L + Q  +++ G AIE R+YAE+P +GFLP+IG LTR R 
Sbjct: 301 EMITGLDLVEWQLRVAAGQALPLKQEQLRIHGHAIEARIYAENPEKGFLPAIGTLTRMRS 360

Query: 361 PAETAAGPLLVNGKWQGDAPSGEAAVRNDTGVYEGGEISMYYDPMIAKLCTWAPTRAAAI 420
            A        V  +    AP   A VR D GV EG  IS +YDPMIAKL  W P R AA+
Sbjct: 361 AA-------AVEFRLGQSAPGDPAHVRIDAGVREGDAISPFYDPMIAKLIVWGPDRDAAL 413

Query: 421 EAMRIALDSFEVEGIGHNLPFLSAVMDHPKFISGDMTTAFIAEEYPEGFEGVNLPETDLR 480
             M+ AL  ++V G+  N+ FL  ++    F +  + T  I       F   + P+T+  
Sbjct: 414 RNMQRALAQYQVVGLATNIAFLQRLVAGQAFSTAALDTGLIERHRDTLFPPPSSPDTETL 473

Query: 481 RVAAAAAAMHRVAEIRRTRVSGRMDNHERRVGTEWVVTLQGADFPVTIAADHDGSTVSFD 540
            +A AA      A+  R+      D   +R G  W +  +      T+  +HD    +  
Sbjct: 474 ALAIAAILQQEHAQAERS------DPWSQRNG--WRLNTR---LLRTLRFEHDAGDTT-- 520

Query: 541 DGSSMRVTSDWTPGDQLANLMVDGAPLVLKVGKISGGFRI-----RTRGADLK-----VH 590
                 V  D+    Q  +L+ +G    L++    G   I     RT  AD+      +H
Sbjct: 521 ------VQLDYAGDGQHWSLLTNGQTHALQLHAADGDTLIISLDGRTLRADVLREGEWLH 574

Query: 591 VRTPRQAELARLMPEKLPPDTSK----MLLCPMPGLIVKVDVEVGQEVQEGQALCTIEAM 646
           V         R +        S+     L  PMPG IV + V+ G  V  G  L  +EAM
Sbjct: 575 VFDAHGQHSLRHVDPLAHAGHSEAEGGRLTAPMPGKIVALLVQKGASVAHGTPLLIMEAM 634

Query: 647 KMENILRAEKKGVVAKINASAGNSLAVDDVIMEFE 681
           KME+ + A   GVV  +  + G+ +A    ++EF+
Sbjct: 635 KMEHTIAAPADGVVEDLLYAVGDQVAEGAQLLEFK 669


Lambda     K      H
   0.317    0.134    0.387 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 1115
Number of extensions: 48
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 681
Length of database: 671
Length adjustment: 39
Effective length of query: 642
Effective length of database: 632
Effective search space:   405744
Effective search space used:   405744
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 54 (25.4 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources