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 |
Related structures:
AlphaFold database: Q4Q1V4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.665 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.556 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.620 |
DOC_CKS1_1 | 233 | 238 | PF01111 | 0.630 |
DOC_CKS1_1 | 382 | 387 | PF01111 | 0.685 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.566 |
DOC_CYCLIN_RxL_1 | 75 | 85 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 331 | 337 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.651 |
DOC_PP1_RVXF_1 | 331 | 338 | PF00149 | 0.635 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.585 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 389 | 399 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 416 | 421 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 7 | 12 | PF00244 | 0.681 |
LIG_Actin_WH2_2 | 257 | 273 | PF00022 | 0.589 |
LIG_BIR_III_2 | 195 | 199 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.642 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.444 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.560 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.629 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.566 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.631 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.633 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.564 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.635 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.679 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.576 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.588 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.563 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.648 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.585 |
LIG_GBD_Chelix_1 | 237 | 245 | PF00786 | 0.602 |
LIG_LIR_Apic_2 | 32 | 38 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.580 |
LIG_MLH1_MIPbox_1 | 425 | 429 | PF16413 | 0.444 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.649 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.579 |
LIG_SH3_1 | 230 | 236 | PF00018 | 0.632 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.695 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.643 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.544 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.700 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.618 |
LIG_SUMO_SIM_anti_2 | 204 | 214 | PF11976 | 0.637 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.661 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.559 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.698 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.633 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.591 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.646 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.522 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.499 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.579 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.668 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.758 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.543 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.608 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.632 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.569 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.548 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.648 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.596 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.576 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.677 |
MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.656 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.627 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.624 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.608 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.657 |
MOD_GlcNHglycan | 355 | 359 | PF01048 | 0.639 |
MOD_GlcNHglycan | 424 | 428 | PF01048 | 0.490 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.576 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.612 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.580 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.725 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.568 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.675 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.659 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.638 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.610 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.569 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.447 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.521 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.561 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.632 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.661 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.697 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.552 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.786 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.701 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.652 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.530 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.780 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.604 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.531 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.554 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.525 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.568 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.698 |
MOD_N-GLC_1 | 72 | 77 | PF02516 | 0.615 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.549 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.669 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.618 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.622 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.591 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.534 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.504 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.482 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.475 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.633 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.737 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.582 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.565 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.538 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.641 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.579 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.524 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.564 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.531 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.590 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.645 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.620 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.585 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.508 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.627 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.571 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.510 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.618 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.558 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.630 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.661 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.611 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.640 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.603 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.632 |
MOD_Plk_2-3 | 27 | 33 | PF00069 | 0.631 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.631 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.628 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.587 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.572 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.601 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.629 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.630 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.604 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.568 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.632 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.770 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.707 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.720 |
MOD_SUMO_for_1 | 400 | 403 | PF00179 | 0.460 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.527 |
TRG_DiLeu_BaEn_2 | 475 | 481 | PF01217 | 0.549 |
TRG_DiLeu_BaEn_4 | 457 | 463 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.572 |
TRG_DiLeu_LyEn_5 | 349 | 354 | PF01217 | 0.647 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.550 |
TRG_NES_CRM1_1 | 461 | 476 | PF08389 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAI1 | Leishmania donovani | 81% | 100% |
A4HNY2 | Leishmania braziliensis | 51% | 100% |
A4ICL2 | Leishmania infantum | 82% | 100% |
E9ASP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |