Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4QGG9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.600 |
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.606 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.479 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.584 |
DEG_COP1_1 | 430 | 439 | PF00400 | 0.545 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.579 |
DOC_CYCLIN_RxL_1 | 187 | 196 | PF00134 | 0.489 |
DOC_CYCLIN_RxL_1 | 76 | 87 | PF00134 | 0.668 |
DOC_CYCLIN_RxL_1 | 93 | 104 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 194 | 200 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 179 | 188 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 494 | 501 | PF00069 | 0.655 |
DOC_MAPK_gen_1 | 93 | 102 | PF00069 | 0.593 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.714 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.637 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.661 |
DOC_USP7_UBL2_3 | 443 | 447 | PF12436 | 0.665 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.697 |
LIG_14-3-3_CanoR_1 | 428 | 437 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 494 | 501 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 66 | 74 | PF00244 | 0.494 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BIR_III_2 | 459 | 463 | PF00653 | 0.535 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 246 | 256 | PF00928 | 0.485 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.595 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.606 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.572 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.529 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.590 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.588 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.454 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.599 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.511 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.544 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.675 |
LIG_LIR_Apic_2 | 317 | 322 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 324 | 334 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 233 | 237 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.541 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.489 |
LIG_REV1ctd_RIR_1 | 335 | 344 | PF16727 | 0.634 |
LIG_SH2_PTP2 | 331 | 334 | PF00017 | 0.400 |
LIG_SH2_SRC | 294 | 297 | PF00017 | 0.647 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.476 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.614 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.598 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 241 | 246 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 369 | 378 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.492 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.574 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.710 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.697 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.548 |
LIG_WW_2 | 21 | 24 | PF00397 | 0.551 |
MOD_CDC14_SPxK_1 | 507 | 510 | PF00782 | 0.597 |
MOD_CDK_SPxK_1 | 193 | 199 | PF00069 | 0.686 |
MOD_CDK_SPxK_1 | 504 | 510 | PF00069 | 0.697 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.550 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.570 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.478 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.846 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.636 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.605 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.594 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.571 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.511 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.558 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.538 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.489 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.668 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.686 |
MOD_CMANNOS | 249 | 252 | PF00535 | 0.483 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.686 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.647 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.682 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.632 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.514 |
MOD_GlcNHglycan | 380 | 385 | PF01048 | 0.767 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.615 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.679 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.535 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.684 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.507 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.588 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.652 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.706 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.532 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.631 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.615 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.578 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.633 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.539 |
MOD_N-GLC_2 | 137 | 139 | PF02516 | 0.498 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.546 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.645 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.570 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.580 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.557 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.534 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.597 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.634 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.660 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.550 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.510 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.616 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.658 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.525 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.639 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.640 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.695 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.578 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.580 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.527 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.602 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.622 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.504 |
MOD_Plk_2-3 | 233 | 239 | PF00069 | 0.510 |
MOD_Plk_2-3 | 35 | 41 | PF00069 | 0.566 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.583 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.673 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.625 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.717 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.577 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.553 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.562 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.653 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.697 |
MOD_SUMO_for_1 | 225 | 228 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 171 | 181 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 218 | 227 | PF00179 | 0.660 |
TRG_DiLeu_BaEn_2 | 229 | 235 | PF01217 | 0.526 |
TRG_DiLeu_BaEn_4 | 270 | 276 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_4 | 485 | 491 | PF01217 | 0.647 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY24 | Leptomonas seymouri | 45% | 92% |
A0A3Q8I9I2 | Leishmania donovani | 82% | 94% |
A4H700 | Leishmania braziliensis | 50% | 100% |
E9AGI4 | Leishmania infantum | 84% | 100% |
E9AP20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |