GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gltI in Pseudomonas simiae WCS417

Align ABC transporter for L-asparagine and L-glutamate, periplasmic substrate-binding component (characterized)
to candidate GFF1096 PS417_05560 ABC transporter

Query= reanno::pseudo1_N1B4:Pf1N1B4_771
         (304 letters)



>FitnessBrowser__WCS417:GFF1096
          Length = 308

 Score =  493 bits (1270), Expect = e-144
 Identities = 248/307 (80%), Positives = 270/307 (87%), Gaps = 4/307 (1%)

Query: 1   MRIVPHILGAAIAAALISTPVFAAELTGTLKKIKESGTITLGHRDASIPFSYIADASGKP 60
           MRIVPHILGAAIAAALISTPVFAAELTGTLKKI +SGTITL HRD+SIPFSYIAD SGKP
Sbjct: 1   MRIVPHILGAAIAAALISTPVFAAELTGTLKKINDSGTITLAHRDSSIPFSYIADGSGKP 60

Query: 61  VGYSHDIQLKIVEAIKKDLDMPNLQVKYNLVTSQTRIPLVQNGTVDVECGSTTNNVERQQ 120
           VGYSHDIQL +VE +KKDL+ P+L+ KYNLVTSQTRIPL+QNGT D+ECGSTTNN ER Q
Sbjct: 61  VGYSHDIQLAVVEQLKKDLNKPDLKAKYNLVTSQTRIPLIQNGTADLECGSTTNNAERAQ 120

Query: 121 QVDFSVGIFEIGTKLLSKKDS----AYKDFADLKGKNVVTTAGTTSERILKSMNADKQMG 176
           QVDF+V IFEIGT+LL KKD     +Y DFADLKGKNVVTTAGTTSERI+K+MNADKQMG
Sbjct: 121 QVDFTVNIFEIGTRLLVKKDKDGKPSYADFADLKGKNVVTTAGTTSERIIKAMNADKQMG 180

Query: 177 MNVISAKDHGESFQMLETGRAVAFMMDDALLAGEMAKAKKPTDWAVTGTAQSNEIYGCMV 236
           MNVISAKDHGESFQMLE+GRAVAFMMDDALLAGE AKAKKP DW +TGT QS E Y CMV
Sbjct: 181 MNVISAKDHGESFQMLESGRAVAFMMDDALLAGEEAKAKKPDDWVITGTPQSFEAYACMV 240

Query: 237 RKGDAPFKKAVDDAIIATYKSGEINKIYEKWFMQPIPPKGLNLMFPMSEELKALIANPTD 296
           RK D  FKKAVDDAI+A YKSGEINKIY KWF  PIPPKGLNL FPMS+++K LIANP+D
Sbjct: 241 RKDDPAFKKAVDDAIVALYKSGEINKIYSKWFESPIPPKGLNLNFPMSDKVKELIANPSD 300

Query: 297 KAADEKK 303
           K A + K
Sbjct: 301 KPAPDVK 307


Lambda     K      H
   0.315    0.131    0.365 

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: 399
Number of extensions: 6
Number of successful extensions: 2
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: 304
Length of database: 308
Length adjustment: 27
Effective length of query: 277
Effective length of database: 281
Effective search space:    77837
Effective search space used:    77837
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 (21.6 bits)
S2: 48 (23.1 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