GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glt in Herbaspirillum seropedicae SmR1

Align Uncharacterized protein (characterized, see rationale)
to candidate HSERO_RS19090 HSERO_RS19090 C4-dicarboxylate ABC transporter

Query= uniprot:A0A0C4Y5S4
         (436 letters)



>FitnessBrowser__HerbieS:HSERO_RS19090
          Length = 431

 Score =  447 bits (1149), Expect = e-130
 Identities = 236/408 (57%), Positives = 306/408 (75%), Gaps = 7/408 (1%)

Query: 10  IFIAMLLGVLAGTAAHHYAPDPAAAKSIADHLSILTDVFLRMIKMIIGPLVFATLVSGIA 69
           IF AMLLG+L G     +  D A AK +A ++SI +D+FLR+IKM+I PLVF+TLV GIA
Sbjct: 11  IFAAMLLGILVGYLIFSHN-DKAQAKELAGYISIASDLFLRLIKMVIAPLVFSTLVVGIA 69

Query: 70  SMGDGKAVGRIGMKAMAWFIAASITSLLLGLLMANLLRPGDGMNLALPAADAA-SNLKTG 128
            MGD K+VGRI  K++AWF  AS+ SL LG++MANLL+PG G+  ALP+ DAA + L T 
Sbjct: 70  HMGDAKSVGRIFGKSLAWFFIASLVSLALGMIMANLLQPGAGV--ALPSPDAAGAGLATS 127

Query: 129 ALNLREFIAHMFPKSFVEAMATNEILQIVVFSLFFGFALGTLKDGIGKPVLAGIEGLSHV 188
              ++EF  H+ PKS VEAMA NE+LQ+VVFS+FFG AL +L +  GK +LA I+ LSH 
Sbjct: 128 KFTVKEFFNHLVPKSIVEAMAQNEVLQVVVFSMFFGIALASLGER-GKHLLAVIDDLSHT 186

Query: 189 MLKITNYVMAFAPVGVFGAVAAVITAEGLGVLVVYAKLLGAVYLSLALLWVALIAGGYFF 248
           MLKIT YVM FAPV VF A+AA +   GL +LV +A  +   Y SL LLWV LIA G+ F
Sbjct: 187 MLKITVYVMKFAPVAVFAAMAATVAVNGLEILVSFAVFMRDFYFSLVLLWVILIAVGFIF 246

Query: 249 LGRDVFRLLKMVRAPLMIGFATASSESAYPKVIEQLGRFGVKERITGFVLPLGYSFNLDG 308
           L + +F LL +++   ++ FATASSE+AYPK+++ L RFGVK +I+ FV+P+GYSFNLDG
Sbjct: 247 LKKRIFHLLALIKEAFLLAFATASSEAAYPKLLDALDRFGVKRKISSFVMPMGYSFNLDG 306

Query: 309 SIMYTSFAALFVAQVYGIHLSLSQQVTMLLVLLVTSKGIAGVPRASLVVVAAVLPMFGLP 368
           S++Y +FA LF+AQ YGIH+ +S Q+TM+LVL++TSKGIAGVPRASLVV+AA L  F +P
Sbjct: 307 SMIYCTFATLFIAQAYGIHMPISTQITMMLVLMLTSKGIAGVPRASLVVIAATLHQFNIP 366

Query: 369 EAGILLVLGIDHVLDMGRTVTNVLGNAIATTVVAKSEGAIGAPVPEEA 416
           EAG+L++LGID  LDMGR+ TN +GN+IA+ VVAK EG  G    EEA
Sbjct: 367 EAGLLVILGIDTFLDMGRSATNAVGNSIASAVVAKWEG--GLMTEEEA 412


Lambda     K      H
   0.325    0.141    0.401 

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: 448
Number of extensions: 21
Number of successful extensions: 4
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: 436
Length of database: 431
Length adjustment: 32
Effective length of query: 404
Effective length of database: 399
Effective search space:   161196
Effective search space used:   161196
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 51 (24.3 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