Align 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized)
to candidate WP_035238778.1 Q366_RS10385 aldehyde dehydrogenase family protein
Query= BRENDA::P23883 (495 letters) >NCBI__GCF_000745975.1:WP_035238778.1 Length = 491 Score = 360 bits (923), Expect = e-104 Identities = 195/479 (40%), Positives = 289/479 (60%), Gaps = 11/479 (2%) Query: 22 LFINGEYTAAAENETFETVDPVTQAPLAKIARGKSVDIDRAMSAARGVFERGDWSLSSPA 81 L+I+G++ A E +TF P L+ A + D+D A+ AAR F+ WS SP Sbjct: 11 LYIDGKWVDAKEGKTFTVTCPANGEFLSTCANAGAEDVDLAVKAARKAFKT--WSQVSPQ 68 Query: 82 KRKAVLNKLADLMEAHAEELALLETLDTGKPIRHSLRDDIPGAARAIRWYAEAIDKVYGE 141 +R +L K+ADL++ AE LA++ETLD GKPIR + D+P A+ R++A A+ G Sbjct: 69 ERAGLLLKIADLIDEKAEHLAMVETLDNGKPIRETRNIDVPLASDHFRYFAGAVRTEEGT 128 Query: 142 VATTSSHELAMIVREPVGVIAAIVPWNFPLLLTCWKLGPALAAGNSVILKPSEKSPLSAI 201 +++++ EP+GVI I+PWNFP L+ WK+ PALAAGN+V++KPS + LS + Sbjct: 129 CTMIDDKTMSIVLSEPIGVIGQIIPWNFPFLMAAWKIAPALAAGNTVVMKPSSDTSLSLL 188 Query: 202 RLAGLAKEAGLPDGVLNVVTGFGHEAGQALSRHNDIDAIAFTGSTRTGKQLLKDAGDSNM 261 A + + LP GV+NVVTG G G A+ H +AFTGST G Q + DA + Sbjct: 189 EFAKIL-DTVLPPGVVNVVTGGGSSTGNAMLNHEGFAKLAFTGSTEVGYQ-IADAAAKKL 246 Query: 262 KRVWLEAGGKSANIVFADCPDLQQAASATAAGIFYNQGQVCIAGTRLLLEESIADEFLAL 321 LE GGKSANI F DCP +A GI +NQGQVC AG+R+ + E I D+FLA Sbjct: 247 IPATLELGGKSANIYFPDCP-WDKAVEGVLLGILFNQGQVCCAGSRVFVHEDIYDKFLAE 305 Query: 322 LKQQAQNWQPGHPLDPATTMGTLIDCAHADSVHSFIREGESKGQLLLDGR---NAGLAAA 378 +K + ++ + G P + T MG I+ A+ + + G+ +G ++ G N G A Sbjct: 306 IKARFESVKVGLPWEEDTMMGAQINLRQAEKILDCVAAGKKEGATVVTGGEKINQGELAK 365 Query: 379 ---IGPTIFVDVDPNASLSREEIFGPVLVVTRFTSEEQALQLANDSQYGLGAAVWTRDLS 435 + PTI DVD + ++++EEIFGPV+ V +F E++ + +AND+ YGLG AVWT+D++ Sbjct: 366 GCFLKPTILADVDNSMTVAQEEIFGPVVCVIKFKDEQEVIDMANDNIYGLGGAVWTKDIN 425 Query: 436 RAHRMSRRLKAGSVFVNNYNDGDMTVPFGGYKQSGNGRDKSLHALEKFTELKTIWISLE 494 RA R++R ++ G ++VN YN PFGGYK+SG GR+ L +++ K I+IS++ Sbjct: 426 RALRVARAVRTGRMWVNTYNQLPAHTPFGGYKKSGIGRETHKMMLAHYSQSKNIYISMD 484 Lambda K H 0.317 0.133 0.389 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: 548 Number of extensions: 19 Number of successful extensions: 6 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: 495 Length of database: 491 Length adjustment: 34 Effective length of query: 461 Effective length of database: 457 Effective search space: 210677 Effective search space used: 210677 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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:
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