GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Cereibacter sphaeroides ATCC 17029

Align proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate WP_011841009.1 RSPH17029_RS07235 FAD-binding oxidoreductase

Query= BRENDA::Q8U022
         (378 letters)



>NCBI__GCF_000015985.1:WP_011841009.1
          Length = 394

 Score =  129 bits (323), Expect = 2e-34
 Identities = 110/364 (30%), Positives = 164/364 (45%), Gaps = 24/364 (6%)

Query: 4   IIGGGIIGVATAYELAKL--GEEVVVFEKR-YFGSGSTFRCASGIRAQFTDEANIKLMKY 60
           +IGG ++G + AY L ++  G +V+V E+   +   ST    + IR QFT   N+ + ++
Sbjct: 10  VIGGAVMGASAAYWLTRMQPGLKVIVVERDPTYARASTALSVASIRMQFTTPVNVAISRF 69

Query: 61  SIERWKTLSEELGHNIMFQ-----QTGYLFLATTEEEVEAFKKNIKLQNKFGVPTRLITP 115
            I   +   E LG  +        + GYLFLA+T E      +   +Q   G  T ++TP
Sbjct: 70  GIGFIREFRESLGQEVGIPSLGLTENGYLFLASTAEGASVLAEVAAMQRSLGAATEMLTP 129

Query: 116 EEAKEIVPPLNADAFLAGAWNPED-GKASPFHTLYAYKKAGERLGVKFYEYTKVVGIEK- 173
                  P L     +AG++ P D G       L  ++ A    GV+F     VVG+E+ 
Sbjct: 130 AALAARFPWLETGDLVAGSFGPRDEGWFDNMGLLNGFRAAARLQGVEFLR-DGVVGLEQA 188

Query: 174 DGSKWKIKTTRGE-FKVDIIINATNAWAREINKMIGKDIIPVTPYKHQL-VKTEPIERGQ 231
            G    ++   GE       INA+   A E+ +M G D +PV P K  + V   P  R  
Sbjct: 189 QGRVRGVRLASGETIACGAAINASGTRAAEVMRMAGLD-LPVEPRKRTVFVIDAPNARHP 247

Query: 232 IEPLVCPPAWNDSYVIQDGEDGGVICGTALEYES--SPDDVTPTYEFVKEVL-KWAVKII 288
             PL+     +  + ++    G  I  T  E +S   P D  P     +EV+ +      
Sbjct: 248 DAPLLV----DRGFYLRPERGGQWITATVPETDSPCDPQDFEPDLHLFEEVVWEQLYARA 303

Query: 289 PALKHVHVVRQWAGHYA-KTPDKNPAIG--MIEENFYVAVGFSGHGFMMAPAVAQALAEK 345
           P    V VVR W GHYA    D+N  +G      N Y+  GFSGHG   APAV + +AE 
Sbjct: 304 PGFDAVKVVRHWVGHYAYNRLDQNAILGPHPALPNLYLMNGFSGHGLQQAPAVGRGIAEH 363

Query: 346 IVEG 349
           ++ G
Sbjct: 364 LLTG 367


Lambda     K      H
   0.318    0.137    0.420 

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: 308
Number of extensions: 15
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: 378
Length of database: 394
Length adjustment: 30
Effective length of query: 348
Effective length of database: 364
Effective search space:   126672
Effective search space used:   126672
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: 50 (23.9 bits)

This GapMind analysis is from Apr 10 2024. 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