GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5404 in Methylocella silvestris BL2

Align ABC transporter for D-Alanine, permease component 1 (characterized)
to candidate WP_012590720.1 MSIL_RS08675 amino acid ABC transporter permease

Query= reanno::pseudo6_N2E2:Pf6N2E2_5404
         (365 letters)



>NCBI__GCF_000021745.1:WP_012590720.1
          Length = 384

 Score =  361 bits (927), Expect = e-104
 Identities = 183/363 (50%), Positives = 248/363 (68%), Gaps = 7/363 (1%)

Query: 8   PDMPPPGSSIGVVAWMRANMFSSWINTLLTLFAFYLIYLIVPPLVQWAILDANWVGTTRA 67
           P  PPP     ++  +  N+F  W  +LLT+  F LI LI PPL+++ + DA W     A
Sbjct: 22  PARPPPPRRRRLIDLIAGNLFDGWRASLLTVATFVLIALITPPLLRFLVFDAVWSAPDGA 81

Query: 68  DCTKEGA--CWVFIQQRFGQFMYGYYPADLRWRVDLTVWLAVIGVAPLFISRFPRKAIYG 125
            C   GA  CW FI ++   F YG YP D RWRVD+T+ +  + +  L      R+ +  
Sbjct: 82  ACRAPGAGACWAFIWRKLPYFTYGSYPLDQRWRVDVTLAIGAVLIFWLLWLDAARRNLAA 141

Query: 126 LSFLVLYPISAWCLLHGGV-FGLDAVATSQWGGLMLTLVIATVGIVGALPLGIVLALGRR 184
           + F  +YP+ A+ LLHG    GL  VA+  WGG+ ++L++A VG+V +LP G++LALGRR
Sbjct: 142 ILFFGVYPVVAFLLLHGAPSIGLPRVASDLWGGIFVSLLVAIVGMVVSLPFGVLLALGRR 201

Query: 185 SNMPAIRVVCVTFIEFWRGVPLITVLFMSSVMLPLFLPEGMNFDKLLRALIGVILFQSAY 244
           S++PA+ + C +FIE  RGVP+ITVLFM++ MLPLF+PE +  D+LLR LIGV LF SAY
Sbjct: 202 SSLPALSIACASFIELVRGVPIITVLFMANTMLPLFVPENLAPDRLLRPLIGVALFASAY 261

Query: 245 IAEVVRGGLQAIPKGQYEAAAAMGLGYWRSMGLVILPQALKLVIPGIVNTFIALFKDTSL 304
           +AEVVRGGLQAIP GQ+E A A+GLG W++  LVILPQAL+ VIPG+VN FIALFKDT+L
Sbjct: 262 MAEVVRGGLQAIPSGQFEGAEALGLGRWQTQRLVILPQALRAVIPGVVNNFIALFKDTTL 321

Query: 305 VIIIGLFDLLNSVKQAAADPKWLG--MATEGYVFAALVFWIFCFGMSRYSMHLERKLDTG 362
           V ++G+FD L +V  A  DP W G  +AT GY FAA+ +++FCF MSRYS+ +ER+    
Sbjct: 322 VAVVGIFDFLRTVDSARLDPVWAGPTIATTGYAFAAMFYFVFCFAMSRYSLFVERRF--S 379

Query: 363 HKR 365
           H+R
Sbjct: 380 HER 382


Lambda     K      H
   0.330    0.144    0.469 

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: 538
Number of extensions: 29
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: 365
Length of database: 384
Length adjustment: 30
Effective length of query: 335
Effective length of database: 354
Effective search space:   118590
Effective search space used:   118590
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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