GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcvT in Pseudomonas fluorescens FW300-N2C3

Align Aminomethyltransferase; EC 2.1.2.10; Glycine cleavage system T protein (uncharacterized)
to candidate AO356_30035 AO356_30035 aminomethyltransferase

Query= curated2:Q7NFJ5
         (359 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_30035
          Length = 376

 Score =  147 bits (372), Expect = 3e-40
 Identities = 117/360 (32%), Positives = 176/360 (48%), Gaps = 30/360 (8%)

Query: 9   LCAQHLQLGARLVPFGGWEMPLQY-STLTREHRAVRTAVGLFDISHMGKYTLSGPDVLAQ 67
           L  +H  LG+ L  + G      Y S L   H+A+RT  GL D+S + K    GP   + 
Sbjct: 10  LAERHRALGSNLEDWNGMGTAWTYDSDLADHHQAIRTRAGLMDVSGLKKVHYVGPHAESL 69

Query: 68  IQRLVPSDLARLQPGQAQYTVLLNEQAGIIDDLIFYCRSPEHWVVIVNGATNDKDRRWLA 127
           +Q     D+A+L PG++ Y  +L+E    +DD I Y   P  ++V V+GA +  +   L 
Sbjct: 70  LQWATTRDIAKLYPGKSVYASMLDEDGKFVDDCIVYRTGPNAFMV-VHGAGSGHE--MLV 126

Query: 128 EHLQG----VHFDDLTGTHTLLALQGPAAVETLQPLVDIDLARLGRFEHAQVSLAGKPAF 183
              QG    V FDD    H  L+LQGP AV+ L   V   + +L  F H Q  L  +P  
Sbjct: 127 RSSQGRQVAVLFDD--DLHD-LSLQGPLAVDFLAEHVP-GIRQLPYFHHLQTRLFDRPVM 182

Query: 184 LARTGYTGEDGFEIMSLEPEGIALWQSL----TAAGVPPCGLGARDTLRLEAAMHLYGQD 239
           ++RTGYTGE G+EI     +  ALW ++       G+ PC   A D LR+E+++  +  D
Sbjct: 183 ISRTGYTGERGYEIFCKAADAPALWDTILEQGAGLGIIPCAFTALDWLRVESSLMFFPYD 242

Query: 240 MDE---------STTPLEASLGWVIDWDKPDYFGREILLAQKAQGTER-RLVGLTVEGRQ 289
             +           T  E  L + +  DK ++ G E     + +G ER ++ G+ +EG +
Sbjct: 243 NSQMYPFADQKAGDTLWEMGLDFTVSPDKREFRGAEEHF--RLRGQERFKITGVLLEGVR 300

Query: 290 IARHGYGLFDGEQQVGVVTSGTLTPTVDRPIALAYVGKPFAPIGSRLEVDIRGRRAMATV 349
            A  G  L+ G QQVGV+T G  +    R +A+A +    +  G  L+V  RG +  A V
Sbjct: 301 AAEAGDTLWQGNQQVGVITCGMYSRLSKRSMAIARMSVACSSPGVALQV--RGSQESAAV 358


Lambda     K      H
   0.321    0.139    0.423 

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: 368
Number of extensions: 23
Number of successful extensions: 5
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: 359
Length of database: 376
Length adjustment: 30
Effective length of query: 329
Effective length of database: 346
Effective search space:   113834
Effective search space used:   113834
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 (21.9 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