GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Pseudomonas fluorescens FW300-N1B4

Align putrescine-pyruvate transaminase (EC 2.6.1.113) (characterized)
to candidate Pf1N1B4_2257 Omega-amino acid--pyruvate aminotransferase (EC 2.6.1.18)

Query= BRENDA::Q9I6J2
         (456 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2257
          Length = 400

 Score =  647 bits (1668), Expect = 0.0
 Identities = 297/371 (80%), Positives = 339/371 (91%)

Query: 7   NAKTREWQALSRDHHLPPFTDYKQLNEKGARIITKAEGVYIWDSEGNKILDAMAGLWCVN 66
           N +TREWQALS DHHL PF+D+KQL EKG RIIT A+GVY+WDSEGNKILD MAGLWCV 
Sbjct: 5   NPQTREWQALSSDHHLAPFSDFKQLKEKGPRIITSAKGVYLWDSEGNKILDGMAGLWCVA 64

Query: 67  VGYGREELVQAATRQMRELPFYNLFFQTAHPPVVELAKAIADVAPEGMNHVFFTGSGSEA 126
           +GYGR+EL  AA++QMRELP+YNLFFQTAHPPV+ELAK I+DVAPEGMNHVFFTGSGSE 
Sbjct: 65  IGYGRDELADAASKQMRELPYYNLFFQTAHPPVLELAKVISDVAPEGMNHVFFTGSGSEG 124

Query: 127 NDTVLRMVRHYWATKGQPQKKVVIGRWNGYHGSTVAGVSLGGMKALHEQGDFPIPGIVHI 186
           NDT+LRMVRHYWA KGQP+KKV+I R NGYHGSTVAG SLGGM  +HEQGD PIPGIVHI
Sbjct: 125 NDTMLRMVRHYWAIKGQPKKKVIISRKNGYHGSTVAGASLGGMTYMHEQGDLPIPGIVHI 184

Query: 187 AQPYWYGEGGDMSPDEFGVWAAEQLEKKILEVGEENVAAFIAEPIQGAGGVIVPPDTYWP 246
           AQPYW+GEGGDM+P+EFG+WAA QLE+KILEVG +NV AFIAEPIQGAGGVI+PPD+YWP
Sbjct: 185 AQPYWFGEGGDMTPNEFGIWAANQLEEKILEVGVDNVGAFIAEPIQGAGGVIIPPDSYWP 244

Query: 247 KIREILAKYDILFIADEVICGFGRTGEWFGSQYYGNAPDLMPIAKGLTSGYIPMGGVVVR 306
           +I+EILAKYDILF+ADEVICGFGRTGEWFG+ +Y   P +M IAKGLTSGYIPMGG++VR
Sbjct: 245 RIKEILAKYDILFVADEVICGFGRTGEWFGTDFYDLKPHMMTIAKGLTSGYIPMGGLIVR 304

Query: 307 DEIVEVLNQGGEFYHGFTYSGHPVAAAVALENIRILREEKIIEKVKAETAPYLQKRWQEL 366
           D++VEVLN+GG+F HGFTYSGHPVAAAVALENIRILR+EKI+E+V+ ETAPYLQKR +EL
Sbjct: 305 DDVVEVLNEGGDFNHGFTYSGHPVAAAVALENIRILRDEKIVERVRTETAPYLQKRLREL 364

Query: 367 ADHPLVGEARG 377
           +DHPLVGE RG
Sbjct: 365 SDHPLVGEVRG 375


Lambda     K      H
   0.320    0.138    0.425 

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: 712
Number of extensions: 29
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: 456
Length of database: 400
Length adjustment: 32
Effective length of query: 424
Effective length of database: 368
Effective search space:   156032
Effective search space used:   156032
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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