GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Cereibacter sphaeroides ATCC 17029

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate WP_043828072.1 RSPH17029_RS08325 ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>NCBI__GCF_000015985.1:WP_043828072.1
          Length = 365

 Score =  279 bits (714), Expect = 8e-80
 Identities = 151/367 (41%), Positives = 224/367 (61%), Gaps = 9/367 (2%)

Query: 12  TRKALTPLLEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQP 71
           T  A   ++E R++ K Y   HA+  +S TI  GE F+LLG SGCGK+TLLR +AGFE+ 
Sbjct: 2   TVAAKPTMIEFRDVHKYYGDYHALRGISATIRAGEFFSLLGPSGCGKTTLLRTIAGFEEI 61

Query: 72  SAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVN 131
           S+G +++DG D   VP   RP NM+FQSYA+FPH+TV +N+ FGL++  L K E   RV 
Sbjct: 62  SSGVVLIDGKDTKGVPANKRPTNMVFQSYAIFPHLTVAENVGFGLRRANLSKEETTRRVA 121

Query: 132 EMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLE 191
           E L +V ++ +  R  H LSGGQRQRVALAR+L  +PK+LLLDEP+ ALDKK+R++MQ+E
Sbjct: 122 EALEMVGLRGYGARAAHALSGGQRQRVALARALILKPKVLLLDEPLSALDKKMREQMQVE 181

Query: 192 VVDILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIG 251
           ++ +  +VG+T ++VTHDQEEA+ M+ RIA+M  G+  Q+ +PE +Y  PT+R  A+FIG
Sbjct: 182 LIKLQRQVGITFILVTHDQEEALVMSDRIAVMFEGEIAQLADPETLYRRPTSRKVADFIG 241

Query: 252 SVNVFEGVLKERQEDGLVLDSPG----LVHPLKVDADASVVDNVPVHVALRPEKIMLCEE 307
           ++N     +      G+ +++ G    L+ P++    AS      V V  RPE   +  E
Sbjct: 242 TMNFLPARILSETGQGIEVEAQGLGRMLLDPMQAPGAAS---GTGVTVGFRPETATILFE 298

Query: 308 PPANGCNFAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRLCW 367
                   A+G +  + Y GD++ Y +RL  G     +L   +   + +   G   R+ W
Sbjct: 299 -GQKADREAMGTIEEVVYYGDMTYYDIRL-DGTEAPIRLSMRNVFGRAVLEIGARARVAW 356

Query: 368 EVDSCVV 374
              + V+
Sbjct: 357 SPGALVL 363


Lambda     K      H
   0.321    0.137    0.400 

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: 343
Number of extensions: 9
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: 377
Length of database: 365
Length adjustment: 30
Effective length of query: 347
Effective length of database: 335
Effective search space:   116245
Effective search space used:   116245
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 Apr 10 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