GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Marinobacter adhaerens HP15

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate GFF1835 HP15_1792 B12-dependent methionine synthase

Query= reanno::Phaeo:GFF1321
         (338 letters)



>FitnessBrowser__Marino:GFF1835
          Length = 1232

 Score =  117 bits (294), Expect = 1e-30
 Identities = 109/363 (30%), Positives = 162/363 (44%), Gaps = 51/363 (14%)

Query: 1   MTNTFTTLLETKDAL-----LADGATGTNLFNMGLQS----GDA-----------PELWN 40
           MT+  T L +   AL     + DG  GT + N+ L      GD             +L N
Sbjct: 1   MTDRTTRLDQLHKALQERIVILDGGMGTMIQNLKLDEKAFRGDRFADYEREVQGNNDLLN 60

Query: 41  VDEPKKITALYQGAVDAGSDLFLTNTFGGTAARLKLHDAHRRVRELNVAGAELGRNVAD- 99
           + +P  +  ++   +DAG+D+  TNTF  T      +      RELNVA AEL R +AD 
Sbjct: 61  LTQPALLRNIHADYLDAGADIIETNTFNSTQLSQADYGLEAIARELNVAAAELARQIADE 120

Query: 100 ----RSERKIAVAGSVGPTG-------EIMQP-VGELSHALAVEMFHEQAEALKEGGVDV 147
                 E+   VAG+VGPT        ++  P    +     V+ ++E    L EGG D+
Sbjct: 121 YTAKNPEKPRFVAGAVGPTSRTASISPDVNNPGYRNVDFQTLVDNYYEAVGGLVEGGCDL 180

Query: 148 LWLETISAPEEYRAAAEAFK--------LADMPWCGTMSFDTAGRTMMGVTSADMAQLVE 199
           + +ETI      +AA  A +           +   GT++ D +GRT+ G T+      V 
Sbjct: 181 ILIETIFDTLNAKAAIYATQQYFEDSGITLPIMISGTIT-DASGRTLSGQTTEAFWNSVA 239

Query: 200 EFDPAPLAFGANCGTGASDILRTVLGFAAQGTTRPIISKGNAGIPKYVDGHIHYDGTPTL 259
                P++ G NC  GA  +   V   +A+  T  + +  NAG+P        YD TP  
Sbjct: 240 H--AKPISVGLNCALGADALRPYVEELSAKAETY-VSAHPNAGLPNEFG---EYDQTPEE 293

Query: 260 MGE-YAAMARDCGAKIIGGCCGTMPDHLRAMREALDTRPRGEQLTLERIVEVLG--PFTS 316
           M E     ARD    IIGGCCG+ PDH+ A+ +A+   P  +     + + + G  PFT 
Sbjct: 294 MAEIIEGFARDGFLNIIGGCCGSRPDHIEAIAQAVSKYPPRKIPERPKALRLSGLEPFTG 353

Query: 317 DSD 319
           D +
Sbjct: 354 DDN 356


Lambda     K      H
   0.317    0.134    0.397 

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: 891
Number of extensions: 49
Number of successful extensions: 3
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: 338
Length of database: 1232
Length adjustment: 38
Effective length of query: 300
Effective length of database: 1194
Effective search space:   358200
Effective search space used:   358200
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: 54 (25.4 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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