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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HXG0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.632 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.627 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.620 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.628 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 443 | 452 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 497 | 501 | PF00244 | 0.617 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.625 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.616 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.664 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.511 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.632 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.675 |
LIG_Integrin_isoDGR_2 | 539 | 541 | PF01839 | 0.716 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 521 | 529 | PF02991 | 0.612 |
LIG_LIR_LC3C_4 | 99 | 104 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.773 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.613 |
LIG_Pex14_1 | 240 | 244 | PF04695 | 0.693 |
LIG_SH2_PTP2 | 260 | 263 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.643 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.642 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.585 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.644 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.601 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.564 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.630 |
LIG_SUMO_SIM_anti_2 | 219 | 226 | PF11976 | 0.526 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.706 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.565 |
MOD_CDK_SPK_2 | 268 | 273 | PF00069 | 0.640 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.553 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.702 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.635 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.590 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.802 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.530 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.627 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.733 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.711 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.621 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.612 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.616 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.544 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.635 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.601 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.632 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.581 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.682 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.667 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.586 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.648 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.572 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.641 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.589 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.628 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.641 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.640 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.609 |
MOD_GlcNHglycan | 487 | 491 | PF01048 | 0.610 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.629 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.627 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.646 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.603 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.706 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.616 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.607 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.741 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.558 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.647 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.779 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.609 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.619 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.615 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.722 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.666 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.769 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.609 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.615 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.712 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.714 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.654 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.587 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.623 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.616 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.553 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.645 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.543 |
MOD_PK_1 | 132 | 138 | PF00069 | 0.626 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.713 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.654 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.595 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.571 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.686 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.619 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.618 |
MOD_PKB_1 | 69 | 77 | PF00069 | 0.730 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.523 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.638 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.613 |
MOD_Plk_2-3 | 21 | 27 | PF00069 | 0.642 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.599 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.523 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.681 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.615 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.604 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.648 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.651 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.621 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.639 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.628 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.697 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 455 | 458 | PF00179 | 0.705 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_4 | 220 | 226 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.521 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 469 | 472 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.727 |
TRG_Pf-PMV_PEXEL_1 | 154 | 158 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 395 | 399 | PF00026 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I516 | Leptomonas seymouri | 57% | 97% |
A0A3Q8IJG5 | Leishmania donovani | 100% | 91% |
A4H946 | Leishmania braziliensis | 85% | 100% |
E9AR55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QEA8 | Leishmania major | 96% | 100% |