GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21216 in Marinobacter adhaerens HP15

Align ABC transporter for D-Glucosamine, ATPase component (characterized)
to candidate GFF4127 HP15_4067 spermidine/putrescine ABC transporter ATPase subunit

Query= reanno::Smeli:SM_b21216
         (360 letters)



>FitnessBrowser__Marino:GFF4127
          Length = 362

 Score =  216 bits (551), Expect = 6e-61
 Identities = 134/360 (37%), Positives = 195/360 (54%), Gaps = 13/360 (3%)

Query: 2   SALEIRNIRKRYGEVETLKGIDIALESGEFLVLLGSSGCGKSTLLNIIAGLAEPSGGDIL 61
           S L    + +R+G    +  + + + +G F  +LG SGCGK+TLL ++AG  +P  GDI 
Sbjct: 3   SDLFCEGLVRRFGSNAAVDHVSLDVPAGTFFSILGPSGCGKTTLLRLLAGFDKPDQGDIH 62

Query: 62  IGERSVLGVHPKDRDIAMVFQSYALYPNLSVARNIGFGLEMRRVPQAEHDKAVRDTARLL 121
           I    +  V P  R + MVFQ  AL+P ++V  NI +GL+ R++P  E  K +      +
Sbjct: 63  IRGERMNDVPPNRRPVNMVFQHLALFPTMTVGDNIAYGLKRRKMPLVERRKRIARVLEQV 122

Query: 122 QIENLLDRKPSQLSGGQRQRVAIGRALVRNPQVFLFDEPLSNLDAKLRMEMRTELKRLHQ 181
            + +L  R P +LSGGQRQRVA+ R LV  P + L DEPL  LD KLR +M+ ELK L +
Sbjct: 123 GLPDLEHRNPQELSGGQRQRVALARCLVLEPTLLLLDEPLGALDLKLREQMKVELKHLQK 182

Query: 182 MLRTTVVYVTHDQIEAMTLATRIAVMRDGRIEQLAAPDEVYDRPATLYVAGFVGSPPMNI 241
              TT VY+THDQ EAM ++ ++AVMRDGR +Q+A P+E+Y  PAT +VAGFVG    N 
Sbjct: 183 QFGTTFVYITHDQSEAMVMSDQVAVMRDGRFDQVAPPEELYREPATPFVAGFVGD--NNR 240

Query: 242 LDAEMTA---NGLKIEGCEEVLPLPAAFNGAAWAGRRVKVGIRPEALRLAAGSEA---QR 295
           L  E+ +   +  ++   + VL      +    AG R ++ IRPE+L L+  + +     
Sbjct: 241 LSGELVSVRDSLAELRLDDGVLVQGRVASDNLQAGHRAELYIRPESLVLSGDALSPGFSS 300

Query: 296 LTASVEVVELTGPELVTTATVGSQRITACLPPRTAVGMGSAHAFTFDGTALHLFDPESGR 355
           + A V      G      A    Q + A LP       GSA   + D +    ++P   R
Sbjct: 301 MQAKVRTTLFDGANSRVEAETCGQPVYARLPQD-----GSAPRLSVDSSIRLAWNPSLAR 355


Lambda     K      H
   0.320    0.136    0.385 

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: 328
Number of extensions: 15
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: 360
Length of database: 362
Length adjustment: 29
Effective length of query: 331
Effective length of database: 333
Effective search space:   110223
Effective search space used:   110223
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: 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