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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HJX4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.683 |
CLV_MEL_PAP_1 | 209 | 215 | PF00089 | 0.524 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 306 | 310 | PF00082 | 0.419 |
CLV_PCSK_FUR_1 | 495 | 499 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.563 |
DEG_APCC_KENBOX_2 | 68 | 72 | PF00400 | 0.535 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.500 |
DOC_PP1_RVXF_1 | 441 | 447 | PF00149 | 0.406 |
DOC_PP2B_LxvP_1 | 245 | 248 | PF13499 | 0.709 |
DOC_PP2B_LxvP_1 | 472 | 475 | PF13499 | 0.633 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 219 | 228 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 536 | 544 | PF00244 | 0.669 |
LIG_14-3-3_CterR_2 | 542 | 547 | PF00244 | 0.491 |
LIG_Actin_WH2_2 | 445 | 460 | PF00022 | 0.412 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.519 |
LIG_CtBP_PxDLS_1 | 242 | 246 | PF00389 | 0.525 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.509 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.607 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.677 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.385 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.479 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.572 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.663 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.584 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.662 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.490 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.535 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 79 | 86 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.531 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.685 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.393 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.427 |
LIG_SH2_SRC | 142 | 145 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.685 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.409 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.661 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.526 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.495 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.470 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 372 | 377 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 91 | 97 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 372 | 377 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 482 | 489 | PF11976 | 0.483 |
LIG_SxIP_EBH_1 | 508 | 522 | PF03271 | 0.488 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.537 |
LIG_TYR_ITIM | 415 | 420 | PF00017 | 0.414 |
LIG_UBA3_1 | 468 | 477 | PF00899 | 0.435 |
LIG_WRC_WIRS_1 | 183 | 188 | PF05994 | 0.526 |
LIG_WW_1 | 248 | 251 | PF00397 | 0.684 |
MOD_CDK_SPK_2 | 540 | 545 | PF00069 | 0.496 |
MOD_CDK_SPK_2 | 64 | 69 | PF00069 | 0.536 |
MOD_CDK_SPxxK_3 | 282 | 289 | PF00069 | 0.680 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.485 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.564 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.599 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.577 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.714 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.613 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.510 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.532 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.536 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.732 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.603 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.619 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.530 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.576 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.643 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.528 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.621 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.536 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.505 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.524 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.667 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.552 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.608 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.500 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.556 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.489 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.745 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.579 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.633 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.533 |
MOD_GlcNHglycan | 272 | 276 | PF01048 | 0.509 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.382 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.638 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.658 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.441 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.579 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.586 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.542 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.658 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.617 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.494 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.598 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.593 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.532 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.600 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.535 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.566 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.620 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.550 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.600 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.477 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.501 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.676 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.709 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.524 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.478 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.535 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.538 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.636 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.582 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.641 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.472 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.473 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.505 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.792 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.531 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.374 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.499 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.547 |
MOD_PK_1 | 497 | 503 | PF00069 | 0.499 |
MOD_PKA_1 | 425 | 431 | PF00069 | 0.501 |
MOD_PKA_1 | 497 | 503 | PF00069 | 0.499 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.535 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.511 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.499 |
MOD_PKB_1 | 495 | 503 | PF00069 | 0.497 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.661 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.592 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.537 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.489 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.514 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.686 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.570 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.560 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.482 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.608 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.647 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.540 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.516 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.543 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.571 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.562 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.749 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.634 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.668 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.483 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.493 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.542 |
MOD_SUMO_for_1 | 446 | 449 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 347 | 355 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 455 | 465 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_2 | 334 | 340 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.687 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6J5 | Leptomonas seymouri | 36% | 94% |
A0A3Q8ICJ1 | Leishmania donovani | 56% | 100% |
A4HJB8 | Leishmania braziliensis | 96% | 100% |
A4I6R1 | Leishmania infantum | 56% | 100% |
E9B1T3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q4Q6C8 | Leishmania major | 55% | 100% |