GapMind for catabolism of small carbon sources

 

Alignments for a candidate for H281DRAFT_01114 in Herbaspirillum seropedicae SmR1

Align deoxynucleoside transporter, substrate-binding component (characterized)
to candidate HSERO_RS05095 HSERO_RS05095 LacI family transcription regulator

Query= reanno::Burk376:H281DRAFT_01114
         (334 letters)



>FitnessBrowser__HerbieS:HSERO_RS05095
          Length = 335

 Score =  476 bits (1224), Expect = e-139
 Identities = 234/326 (71%), Positives = 267/326 (81%), Gaps = 1/326 (0%)

Query: 10  LAAAALTVGVIAAAQAATNET-IVTVVKVTGINWFNRMDEGVKEFAKDNPGVTAYQTGPG 68
           L +A   VG  +A QA      IVTVVK+TGI+WFNRM+ GVKEFA  NPGVT  Q GP 
Sbjct: 10  LVSALAAVGFASALQAQNKPIDIVTVVKITGISWFNRMEVGVKEFAAANPGVTTRQIGPA 69

Query: 69  RADAAQQLKIIEDLIAKKVNAIAVVPYDPPTLEPALKKAMDRGIKVVTHEADNAKNTMVD 128
           ++DAAQQ +++EDL+AKKV+AIAVV  DPPTLEP LK+A+DRGIKVVTHEADN KNT+VD
Sbjct: 70  QSDAAQQQRLVEDLVAKKVDAIAVVSMDPPTLEPVLKRALDRGIKVVTHEADNQKNTLVD 129

Query: 129 IEAFDNTAYGAGLNERLASCMHNEGKWAVLVGSLGSRSQVQWADGGIGNAKAKYAKMNLV 188
           IEAFDNTAYGA LN+RLA+CM   GKW+ LVGSLGS+SQVQWADGG  NA  KY KM LV
Sbjct: 130 IEAFDNTAYGARLNDRLAACMGQAGKWSSLVGSLGSQSQVQWADGGAANAAKKYPKMTLV 189

Query: 189 EPKLETNNDGERAYEVAKEVLRKHPDLKGFQGSSSLDVIGIGRAVEEAGMQGKICVYGTG 248
           + K E+ ND E+AY  AKE+LRKHPD+KGFQGSSSLDV+GIGRAVEEAG+QGK+CVYGTG
Sbjct: 190 DAKNESANDAEKAYAKAKEILRKHPDIKGFQGSSSLDVLGIGRAVEEAGLQGKVCVYGTG 249

Query: 249 LPTEAGKFLESGAINGIAFWDPKLAGIAMNKVAKMLVDGKTVENGADLGIPGYTKVTVAK 308
           LP+EA KFLESGA+ GIAFWDPK AG+AMNK A MLV GK + +G DLGIPGY KVTV K
Sbjct: 250 LPSEAAKFLESGAVGGIAFWDPKDAGLAMNKAAMMLVQGKKITDGMDLGIPGYNKVTVKK 309

Query: 309 GPGKGIIVRGQGWVNVDKSNYKQYPF 334
           GPG G+IV GQ WV VDK NYKQY F
Sbjct: 310 GPGVGVIVTGQAWVEVDKKNYKQYAF 335


Lambda     K      H
   0.314    0.133    0.385 

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: 427
Number of extensions: 12
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 334
Length of database: 335
Length adjustment: 28
Effective length of query: 306
Effective length of database: 307
Effective search space:    93942
Effective search space used:    93942
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: 42 (22.0 bits)
S2: 49 (23.5 bits)

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

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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:

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:

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:

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:

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