This is a highly disordered Cys-rich prote8in with spurious hydrophobic segments. Very low conservation.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032299 | ribonuclease H2 complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
Related structures:
AlphaFold database: A4H6Y6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 499 | 503 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 72 | 76 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 99 | 103 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.329 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.534 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 496 | 500 | PF00917 | 0.492 |
DOC_CDC14_PxL_1 | 34 | 42 | PF14671 | 0.538 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.231 |
DOC_CYCLIN_yCln2_LP_2 | 197 | 203 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 246 | 254 | PF00069 | 0.310 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.698 |
DOC_PP4_FxxP_1 | 107 | 110 | PF00568 | 0.544 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 473 | 481 | PF00244 | 0.316 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 341 | 345 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.535 |
LIG_CtBP_PxDLS_1 | 320 | 324 | PF00389 | 0.310 |
LIG_EVH1_2 | 291 | 295 | PF00568 | 0.231 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.532 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.328 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.659 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.608 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.699 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.310 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.545 |
LIG_Integrin_isoDGR_2 | 185 | 187 | PF01839 | 0.539 |
LIG_Integrin_RGD_1 | 63 | 65 | PF01839 | 0.556 |
LIG_LIR_Apic_2 | 509 | 515 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 377 | 387 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.476 |
LIG_MLH1_MIPbox_1 | 434 | 438 | PF16413 | 0.535 |
LIG_NRBOX | 327 | 333 | PF00104 | 0.304 |
LIG_PDZ_Class_3 | 514 | 519 | PF00595 | 0.317 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.231 |
LIG_Pex14_2 | 380 | 384 | PF04695 | 0.474 |
LIG_SH2_NCK_1 | 84 | 88 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 95 | 99 | PF00017 | 0.486 |
LIG_SH2_SRC | 119 | 122 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.239 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.496 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.496 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.537 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.539 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.459 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.242 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.269 |
LIG_SUMO_SIM_par_1 | 319 | 324 | PF11976 | 0.335 |
LIG_WW_3 | 3 | 7 | PF00397 | 0.552 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.575 |
MOD_CDK_SPxxK_3 | 438 | 445 | PF00069 | 0.531 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.540 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.659 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.669 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.241 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.675 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.617 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.526 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.658 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.534 |
MOD_CMANNOS | 454 | 457 | PF00535 | 0.350 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.541 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.621 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.647 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.600 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.247 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.332 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.384 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.704 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.758 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.622 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.485 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.520 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.688 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.569 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.663 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.500 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.602 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.590 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.327 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.667 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.560 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.548 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.470 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.364 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.507 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.498 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.272 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.478 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.279 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.528 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.605 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.535 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.510 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.342 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.740 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.526 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.510 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.675 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.221 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.369 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.605 |
MOD_Plk_2-3 | 41 | 47 | PF00069 | 0.544 |
MOD_Plk_2-3 | 73 | 79 | PF00069 | 0.543 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.231 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.231 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.289 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.525 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.549 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.574 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.310 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.562 |
TRG_DiLeu_BaEn_2 | 375 | 381 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 473 | 478 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 482 | 486 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q4 | Leptomonas seymouri | 39% | 79% |
A4H708 | Leishmania braziliensis | 98% | 77% |
Q4QGI7 | Leishmania major | 48% | 100% |
Q4QGK9 | Leishmania major | 50% | 100% |