GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Azospirillum brasilense Sp245

Align TRAP-type periplasmic solute-binding protein (characterized, see rationale)
to candidate AZOBR_RS26640 AZOBR_RS26640 ABC transporter substrate-binding protein

Query= uniprot:Q930R1
         (334 letters)



>FitnessBrowser__azobra:AZOBR_RS26640
          Length = 339

 Score =  370 bits (950), Expect = e-107
 Identities = 177/330 (53%), Positives = 241/330 (73%), Gaps = 1/330 (0%)

Query: 5   LLATTAIAFGLSAAAPAFAEFNDRNIRVSNGINEDHPVGNGIKAMQACLDQKSGGKLKLT 64
           ++ T A+A  L AAAPA A+  +R +R+S  + +DHP   G+ A+ AC  +KSGGK+K+ 
Sbjct: 8   IILTVAVA-ALFAAAPAKAQTAERTMRLSAAVAQDHPFAAGVSALTACAAEKSGGKMKIQ 66

Query: 65  AFWGGALGGDLQATQALRSGVQEAVVTSSSPLVGIIPALGVFDLPFLFANAQEAYTVLDG 124
           +FW  ALG D+QA Q +R G  + VV S+SPL  ++PA+GVFDLPFLF N  EA  +LDG
Sbjct: 67  SFWNAALGSDMQAVQLVRGGSLDMVVASTSPLASLVPAMGVFDLPFLFENETEADRILDG 126

Query: 125 DFGDMMNEKLEAAGLVNLAYWENGFRNLSNSVRPVTKWEDFEGMKVRVMQNNIFLDTFQN 184
             G  ++EKL+  GLVNLAYWENGFRNL+NS RP+ KWED  G K+RVMQN +F+DTF  
Sbjct: 127 AVGQQLSEKLQGVGLVNLAYWENGFRNLTNSRRPIQKWEDLGGTKIRVMQNPVFMDTFST 186

Query: 185 LGANATPMAFGEVFSALETKAIDAQENPYVTIDTSKFFEVQKYVTETNHAYTPFLFLFSK 244
           LGANA PMAF E+F+ALET+A+D QENPY  I+T KF+E QKY++ TNHAYTP + L+SK
Sbjct: 187 LGANAVPMAFSELFTALETRAVDGQENPYANIETGKFYEAQKYLSVTNHAYTPAVILYSK 246

Query: 245 PIFDSYTPEEQAALRECAVVGRDEERKVIQDLNKKSLEKIKEAGLEVNTLSAEEQARIRE 304
            I+D  +  E+  L+ CA V R EER+V ++ ++KSL ++K+ G++VN LSAEE+ R+ +
Sbjct: 247 KIWDGLSSAERDVLQSCAAVARTEERRVNREQSEKSLARLKDLGMQVNELSAEERKRMLQ 306

Query: 305 KSMVVYEKHKAEIGAEVVDAILAKLEEIRK 334
           K   VYEKH A IGAE +  + ++L ++RK
Sbjct: 307 KVAPVYEKHAATIGAETMTLLQSELGQLRK 336


Lambda     K      H
   0.317    0.133    0.374 

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: 305
Number of extensions: 13
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: 339
Length adjustment: 28
Effective length of query: 306
Effective length of database: 311
Effective search space:    95166
Effective search space used:    95166
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: 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