GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07300 in Herbaspirillum seropedicae SmR1

Align Inositol transport system sugar-binding protein (characterized)
to candidate HSERO_RS12110 HSERO_RS12110 sugar ABC transporter substrate-binding protein

Query= reanno::Phaeo:GFF715
         (316 letters)



>FitnessBrowser__HerbieS:HSERO_RS12110
          Length = 331

 Score =  326 bits (836), Expect = 4e-94
 Identities = 161/335 (48%), Positives = 220/335 (65%), Gaps = 32/335 (9%)

Query: 10  LATTVAAAPMMLATTASAEGEKYILVSHAPDSDSWWNTIKNGIALAGEQMNVEVEYRNPP 69
           +A   AA P    + + A  E+++L+SHAPDSDSWWNTIKN I  AGE  +V V+YRNP 
Sbjct: 1   MALLAAATP----SPSVAANERFVLISHAPDSDSWWNTIKNAIKQAGEDFDVSVDYRNPS 56

Query: 70  TGDLADMARIIEQAAASGPNGIITTLSDYDVLSGPIKAAVDSGVDVIIMNSGTPDQAREV 129
            GDLADMAR++EQAAA   NG++ +++D+ VL  PI+  V   + VI +NSGT  Q+ ++
Sbjct: 57  NGDLADMARLVEQAAARNYNGVVVSIADFSVLKKPIEMVVAKNIPVITINSGTQQQSEQL 116

Query: 130 GALMYVGQPEYDAGHAAGMRAKADGVGSFLCVNHYISSPSSTERCQGFADGLGVDLGDQM 189
           GALM+VGQPEYDAG+ AG +AKA G+ SFLCVNHY ++PSS ERC+GFA+ +G D     
Sbjct: 117 GALMHVGQPEYDAGYGAGQKAKAAGIKSFLCVNHYATNPSSFERCRGFAEAIGADYKKST 176

Query: 190 IDSGQDPAEIKNRVLAYLNTNPETDAILTLGPTSADPTLLALDENGMAGDIYFGTFDLGE 249
           +D+G DP  ++++V AYL  NP T A+L LGP SA P+L AL + G+   I+F TFDL E
Sbjct: 177 LDTGIDPNAVESKVSAYLRNNPGTQAVLALGPDSAVPSLRALQKMGLKSKIWFATFDLSE 236

Query: 250 EIVKGLKSGVINWGIDQQPFLQAYLPVVVLT-------------------------NYHR 284
           EI  G+K G + + IDQQP+LQ Y+PV +L                              
Sbjct: 237 EIANGIKDGSVQFAIDQQPYLQGYIPVAILALSRQLKTNDVAVLQDKLKGNAKFQARLAE 296

Query: 285 YGVLP---GNNINSGPGFVTKDGLEKVEEFAGEYR 316
           YG+ P     +I+SGPG++T+D L+KV ++AG+YR
Sbjct: 297 YGLAPIYGPRHISSGPGYITRDNLDKVLKYAGQYR 331


Lambda     K      H
   0.315    0.134    0.393 

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: 348
Number of extensions: 10
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 316
Length of database: 331
Length adjustment: 28
Effective length of query: 288
Effective length of database: 303
Effective search space:    87264
Effective search space used:    87264
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: 48 (23.1 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